関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hexachloroethane | HCID 6214 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Triphenylphosphine | HCID 11776 | — |
| 反応物 | (2S,4R)-4-tert-butoxy-2-(2-oxo-ethylcarbamoyl)-pyrrolidine-1-carboxylic acid benzyl ester | HCID 59548499 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | (2S,4R)-4-tert-butoxy-2-oxazol-2-yl-pyrrolidine-1-carboxylic acid benzyl ester | HCID 59548492 | 46.7% |
反応手順
To a stirred solution of (2S,4R)-4-tert-butoxy-2-(2-oxo-ethylcarbamoyl)-pyrrolidine-1-carboxylic acid benzyl ester (4.5 g, 12.43 mmol) and hexachloroethane (5.88 g, 24.86 mmol) in dichloromethane (30 mL) was added triphenyl phosphine (6.52 g, 24.86 mmol) The mixture was stirred at 0° C. for 15 min, triethylamine (2.5 g, 24.86 mmol) was then added and the mixture was stirred at room temp. for 14 h. The reaction mixture was then extracted with dichloromethane and washed with water and brine. The organic layer was dried over anhydrous sodium sulfate and concentrated. The residue was purified by column chromatography (using 15% EtOAc in hexane as eluent) to give (2S,4R)-4-tert-butoxy-2-oxazol-2-yl-pyrrolidine-1-carboxylic acid benzyl ester (2 g, 46.6% yield) as a yellow liquid. MS calcd. for C19H25N2O4 [(M+H)+] 345.0, obsd. 345.2.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09090559B2 |
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| 出典データセット | uspto-grants-2015_07 |
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| ORD ID | ord-0a1694a9d5c4432f8ad7a09c31456988 |
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| 出典メモ | uspto-grants-2015_07 |
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