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8th February 2011 @ 00:52
Preparation of starting material for the [url=http://www.thesynapticleap.org/node/317]Ugi reaction[/url] via an alternative route to [url=http://www.ourexperiment.org/racemic_pzq/309][b]MW34-1[/b][/url] See also: [*] [url=http://www.ourexperiment.org/racemic_pzq/338]Upscaling - Preparation of 2-Phenylethyl isocyanide (MW34-2)[/url] [*] [url=http://www.ourexperiment.org/racemic_pzq/357]Preparation of 2-(3,4-Dimethoxyphenyl)ethyl isocyanide (MW37)[/url] [*] [url=http://www.ourexperiment.org/racemic_pzq/338/]Scale-up - Preparation of 2-Phenylethyl isocyanide (MW34-2)[/url] [data=size:500x150]771[/data] [b]Hazard and Risk Assessment:[/b] [data]773[/data] Start time: 11:50 AM 08/02/2011 End time: 7:00 PM 09/02/2011 A solution of 2-phenylethylamine (5.00 g, 41.3 mmol, M.W. 121.2 g/mol) was heated to reflux in ethyl formate (25 mL, M.W. 74.1 g/mol, bp 52-54°C) and heated to reflux for 21 h. Reaction control via TLC showed a complete consumption of the starting material (hexane:ethyl acetate = 1:1, stain: KMnO4, Rf [starting material]=0.05, Rf [product]=0.25). The remaining ethyl formiate and the by-product ethanol were removed under reduced pressure obtaining 2-phenylethylformamide as a yellow liquid. 2-phenylethylformamide and triethylamine (12.5g, 124 mmol, 17 mL, 3.0 eq., M.W. 101.2, d=0.726 g/mL) were dissoved in dry DCM (50 mL) and phosphoryl chloride (41.3 mmol, 6.32 g, 3.84 mL, 1.0 eq., M.W. 153.3, d=1.645 g/mL) was dropwise added at 0°C. The mixture was stirred for 1 h at 0°C and a further 4 h at room temperature. - quenched with water - neutralized with NaHCO3, acidic wash (difficult separation of the layers) - evaporated, dried over magnesium sulfate [u]Crude yield:[/u] 5.41 g (41.2 mmol, 100%) dark brown liquid [M.W. 131.2 g/mol] 1H NMR: [data=text]775[/data]: small solvent impurities (triethylamine?) Purification: Column chromatography (silica gel, hexane:ethyl acetate = 4:1; Rf = 0.5) Yield 4.42 g (33.7 mmol, 82%) yellow liquid [u]Note:[/u] Store 2-phenylethyl isocyanide in the freezer at -20°C. [b]Procedure from reference: [1][/b] ([i]translated from German[/i]) [u]Example 2: 2-phenylethyl isocyanide[/u] Phenylethylamine is heated at reflux temperature in ethyl formiate (excess) for several hours. The solvent and the ethanol by-product are evaporated and to give 2-aminophenylethyl formiate in a qunatiative yield. The formiat is dissolved in DCM and 3 equivalents of triethylamine are added. The mixture is cooled to 0°C and 1 equivalent of phosphoryl chloride is added slowly and stirred at this temperature for 2 h and a further 3 h at room temperature. The reaction is quenched by addition of water and neutralized to pH 8 by addition of NaHCO3. The organic layer is seperated and the aqueous layer is extracted with dichloromethane several times. The combined organic layers are dried and evaporated to obtain 2-phenylethyl isocyanide in a relatively pure form and can be used directly in the next step. Alternatively, 2-phenylethyl isocyanide can be distilled under vacuum. Yield 65%. [b]References:[/b] [url=http://v3.espacenet.com/publicationDetails/biblio?CC=WO&NR=2009115333A1&KC=A1&FT=D&date=20090924&DB=EPODOC&locale=en_ep][1] “Novel Synthesis of Praziquantel“, A. Dömling, [i]Patent Application[/i] [b]2009[/b], WO 2009/11533(A1), Language: German.[/url]
Attached Files
Scheme MW34-3.png
HRAF MW34-3.pdf
1H NMR MW34-3.pdf
1H NMR MW34-3 JCAMP-DX.dx