関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | tert-Butyl methyl ether | HCID 15413 | — |
| 反応物 | Methyl 1-(4-hydroxyphenyl)-5-oxopyrrolidine-3-carboxylate | HCID 2883518 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Phosphate | HCID 1061 | — |
| 溶媒 | Sodium Sulfate | HCID 24436 | — |
| 生成物 | (R)-1-(4-hydroxyphenyl)-5-oxo-pyrrolidine-3-carboxylic acid methyl ester | HCID 785702 | — |
反応手順
A suspension of 2.51 g (10.6 mmol) of (RS)-1-(4-hydroxy-phenyl)-5-oxo-pyrrolidine-3-carboxylic acid methyl ester in 10 ml of phosphate buffer [c(KH2PO4)=0.05 mol/l], 25 ml of sodium sulfate solution [c(Na2SO4)=4 mol/l], 45 ml of deionised water, and 20 ml of tert-butylmethylether is adjusted to pH 6.0. Under moderate stirring, 51.3 mg of cholesterase from Candida cylindracea (Roche Applied Science, Industrial Products, Enzyme Projects, Sandhofer Str. 116, D-68305 Mannheim, Germany, order no. 10129046103) are added in solid form. By an automatic pH-Stat-System, the pH is kept constant at 6.0 by addition of sodium hydroxide solution [c(NaOH)=1.0 mol/l] at RT. The progress of the reaction is followed by the consumption of sodium hydroxide solution. After the addition of 5.21 ml of sodium hydroxide solution, the reaction is stopped by addition of dichloromethane. The organic layer is separated, then washed three times with water, thereafter, dried over sodium sulfate, and finally evaporated. The crude ester is a slightly rose oil which after trituration in tert-butylmethylether at RT is obtained as a white solid. The product is collected on a filter funnel and yields after drying under high vacuum at RT 1.11 g (44.3% of theory) of (R)-1-(4-hydroxy-phenyl)-5-oxo-pyrrolidine-3-carboxylic acid methyl ester; m.p.: 122.9° C.; optical integrity: 97.9% e.e.; [α]20D=−35.2 (c=1.162 g/100 ml CHCl3).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07122562B2 |
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| 出典データセット | uspto-grants-2006_10 |
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| ORD ID | ord-1f5004ad4eb849b6ae7b47c0a54d6276 |
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| 出典メモ | uspto-grants-2006_10 |
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