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51976447Preparation of (2-isocyanoethyl)benzene (MNR21-4)
Experiments
plus.google.com-113014781212630252105Murray Robertson [url=http://onlinelibrary.wiley.com/doi/10.1002/chem.201002046/abstract;jsessionid=723FBA3B0C773C23E60CDC106E8C9FC1.d02t03?systemMessage=Wiley+Online+Library+will+be+disrupted+24+March+from+10-14+GMT+%2806-10+EDT%29+for+essential+maintenance]DOI: 10.1002/chem.201002046[/url] [b]Hazard and Risk Assessment:[/b] [data]3737[/data] Water (60 mL) was added to a 500 mL round-bottomed flask. Sodium hydroxide (60.0 g, 1.5 mol) was added portionwise followed by a mixture of 2-phenylethylamine (24.3 mL, 0.19 mol), chloroform (16.0 mL, 0.19 mol), and benzyltriethylammonium chloride (400 mg, 1.8 mmol) in dichloromethane (60 mL)dropwise over 10 mins. The reaction mixture was then refluxed for 4 hours. The reaction mixture was then allowed to cool to room temperature and was diluted with ice and water (50 mL), the organic layer was separated and retained, the aqueous layer was extracted with DCM (2 x 60 mL). The organic fractions were then combined and washed with HCl (1M) (3 x 100 mL) and brine (100 mL), dried over anhydrous magnesium sulfate, filtered and concentrated to give the crude as a dark orange oil (23.90 g) The crude was passed through a short column (60-100 EtOAC) collecting the top running spot. After concentration, (2-isocyanoethyl)benzene (MNR21-4) was afforded as a dark yellow oil (17.618 g, 134.31 mmol, 70%) [b]Characterisation[/b] [data]4910[/data][data]4912[/data] 1H NMR (400 MHz, CDCl3): d = 7.37-7.21 (m, 5H), 3.60 (tt, J = 10.6, 1.9 Hz, 2H), 2.98 (tt, J = 10.6, 1.9 Hz, 2H) [data]188[/data] 13C NMR – MW34-1 (50 MHz, CDCl3): d = 156.6, 136.7, 128.7, 128.7, 127.2, 42.9 (t, J = 6.5) 35.6. [data]192[/data] Vmax/cm-1 2147, 1454 [blog]309[/blog] *lab book entry closed]]>Mnr: 21-30
Repeat of MNR21-3 on the same scale.





DOI: 10.1002/chem.201002046

Hazard and Risk Assessment:
HIRAC MNR23-3.pdf


Water (60 mL) was added to a 500 mL round-bottomed flask. Sodium hydroxide (60.0 g, 1.5 mol) was added portionwise followed by a mixture of 2-phenylethylamine (24.3 mL, 0.19 mol), chloroform (16.0 mL, 0.19 mol), and benzyltriethylammonium chloride (400 mg, 1.8 mmol) in dichloromethane (60 mL)dropwise over 10 mins. The reaction mixture was then refluxed for 4 hours.

The reaction mixture was then allowed to cool to room temperature and was diluted with ice and water (50 mL), the organic layer was separated and retained, the aqueous layer was extracted with DCM (2 x 60 mL). The organic fractions were then combined and washed with HCl (1M) (3 x 100 mL) and brine (100 mL), dried over anhydrous magnesium sulfate, filtered and concentrated to give the crude as a dark orange oil (23.90 g) The crude was passed through a short column (60-100 EtOAC) collecting the top running spot. After concentration, (2-isocyanoethyl)benzene (MNR21-4) was afforded as a dark yellow oil (17.618 g, 134.31 mmol, 70%)

Characterisation

mnr21-4_1H.pdf
mnr21-4_frac1.zip


1H NMR (400 MHz, CDCl3): d = 7.37-7.21 (m, 5H), 3.60 (tt, J = 10.6, 1.9 Hz, 2H), 2.98 (tt, J = 10.6, 1.9 Hz, 2H)

13C NMR MW34-1


13C NMR – MW34-1 (50 MHz, CDCl3): d = 156.6, 136.7, 128.7, 128.7, 127.2, 42.9 (t, J = 6.5) 35.6.

IR MW34-1


Vmax/cm-1 2147, 1454

Preparation of 2-Phenylethyl isocyanide (MW34-1)

*lab book entry closed
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]]>2012-03-22T06:12:28+00:002012-08-25T03:02:20+01:0063f80fb9b94149cbb5e63482a47f128c721-30https://www.ourexperiment.org/data/4910.xmlhttps://www.ourexperiment.org/data/4912.xmlhttp://www.ourexperiment.org/uri/22dhttps://www.ourexperiment.org/racemic_pzq/5197/Preparation_of_2isocyanoethylbenzene_MNR214.htmlhttps://www.ourexperiment.org/racemic_pzq/5197/Preparation_of_2isocyanoethylbenzene_MNR214.htmlhttps://www.ourexperiment.org/racemic_pzq/5197/Preparation_of_2isocyanoethylbenzene_MNR214.xmlhttps://www.ourexperiment.org/racemic_pzq/5197/Preparation_of_2isocyanoethylbenzene_MNR214.pnghttps://www.ourexperiment.org/racemic_pzq/5197/Preparation_of_2isocyanoethylbenzene_MNR214.xml?revision=5197https://www.ourexperiment.org/racemic_pzq/5197/Preparation_of_2isocyanoethylbenzene_MNR214.xml?revision=5200https://www.ourexperiment.org/racemic_pzq/5197/Preparation_of_2isocyanoethylbenzene_MNR214.xml?revision=6443https://www.ourexperiment.org/racemic_pzq/5197/Preparation_of_2isocyanoethylbenzene_MNR214.xml?revision=6444https://www.ourexperiment.org/racemic_pzq/5197/Preparation_of_2isocyanoethylbenzene_MNR214.xml?revision=6445https://www.ourexperiment.org/racemic_pzq/5197/Preparation_of_2isocyanoethylbenzene_MNR214.xml?revision=6446https://www.ourexperiment.org/racemic_pzq/5197/Preparation_of_2isocyanoethylbenzene_MNR214.xml?revision=6447https://www.ourexperiment.org/racemic_pzq/5197/Preparation_of_2isocyanoethylbenzene_MNR214.xml?revision=7104
51977104Preparation of (2-isocyanoethyl)benzene (MNR21-4)
Experiments
plus.google.com-113014781212630252105Murray Robertson [url=http://onlinelibrary.wiley.com/doi/10.1002/chem.201002046/abstract;jsessionid=723FBA3B0C773C23E60CDC106E8C9FC1.d02t03?systemMessage=Wiley+Online+Library+will+be+disrupted+24+March+from+10-14+GMT+%2806-10+EDT%29+for+essential+maintenance]DOI: 10.1002/chem.201002046[/url] [b]Hazard and Risk Assessment:[/b] [data]3737[/data] Water (60 mL) was added to a 500 mL round-bottomed flask. Sodium hydroxide (60.0 g, 1.5 mol) was added portionwise followed by a mixture of 2-phenylethylamine (24.3 mL, 0.19 mol), chloroform (16.0 mL, 0.19 mol), and benzyltriethylammonium chloride (400 mg, 1.8 mmol) in dichloromethane (60 mL)dropwise over 10 mins. The reaction mixture was then refluxed for 4 hours. The reaction mixture was then allowed to cool to room temperature and was diluted with ice and water (50 mL), the organic layer was separated and retained, the aqueous layer was extracted with DCM (2 x 60 mL). The organic fractions were then combined and washed with HCl (1M) (3 x 100 mL) and brine (100 mL), dried over anhydrous magnesium sulfate, filtered and concentrated to give the crude as a dark orange oil (23.90 g) The crude was passed through a short column (60-100 EtOAC) collecting the top running spot. After concentration, (2-isocyanoethyl)benzene (MNR21-4) was afforded as a dark yellow oil (17.618 g, 134.31 mmol, 70%) [b]Characterisation[/b] [data]4910[/data][data]4912[/data] 1H NMR (400 MHz, CDCl3): d = 7.37-7.21 (m, 5H), 3.60 (tt, J = 10.6, 1.9 Hz, 2H), 2.98 (tt, J = 10.6, 1.9 Hz, 2H) [data]188[/data] 13C NMR – MW34-1 (50 MHz, CDCl3): d = 156.6, 136.7, 128.7, 128.7, 127.2, 42.9 (t, J = 6.5) 35.6. [data]192[/data] Vmax/cm-1 2147, 1454 [blog]309[/blog] *lab book entry closed]]>Mnr: 21-30
Repeat of MNR21-3 on the same scale.





DOI: 10.1002/chem.201002046

Hazard and Risk Assessment:
HIRAC MNR23-3.pdf


Water (60 mL) was added to a 500 mL round-bottomed flask. Sodium hydroxide (60.0 g, 1.5 mol) was added portionwise followed by a mixture of 2-phenylethylamine (24.3 mL, 0.19 mol), chloroform (16.0 mL, 0.19 mol), and benzyltriethylammonium chloride (400 mg, 1.8 mmol) in dichloromethane (60 mL)dropwise over 10 mins. The reaction mixture was then refluxed for 4 hours.

The reaction mixture was then allowed to cool to room temperature and was diluted with ice and water (50 mL), the organic layer was separated and retained, the aqueous layer was extracted with DCM (2 x 60 mL). The organic fractions were then combined and washed with HCl (1M) (3 x 100 mL) and brine (100 mL), dried over anhydrous magnesium sulfate, filtered and concentrated to give the crude as a dark orange oil (23.90 g) The crude was passed through a short column (60-100 EtOAC) collecting the top running spot. After concentration, (2-isocyanoethyl)benzene (MNR21-4) was afforded as a dark yellow oil (17.618 g, 134.31 mmol, 70%)

Characterisation

mnr21-4_1H.pdf
mnr21-4_frac1.zip


1H NMR (400 MHz, CDCl3): d = 7.37-7.21 (m, 5H), 3.60 (tt, J = 10.6, 1.9 Hz, 2H), 2.98 (tt, J = 10.6, 1.9 Hz, 2H)

13C NMR MW34-1


13C NMR – MW34-1 (50 MHz, CDCl3): d = 156.6, 136.7, 128.7, 128.7, 127.2, 42.9 (t, J = 6.5) 35.6.

IR MW34-1


Vmax/cm-1 2147, 1454

Preparation of 2-Phenylethyl isocyanide (MW34-1)

*lab book entry closed
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