関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| 反応物 | 2-Phenylpropionic acid | HCID 10296 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | Ethanedioic acid, monoethyl ester | HCID 21943339 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Hexane | HCID 8058 | — |
| 生成物 | ethyl(RS)-2-oxo-3-phenylbutyrate | HCID 11435685 | 97% |
反応手順
A 1.6 N solution of n-butyllithium in hexane was run dropwise into a solution, cooled to the region of −70° C., of 33 g (0.220 mol) of (RS)-2-phenylpropionic acid in 220 cm3 of tetrahydrofuran and of 44 cm3 of N,N′-tetramethylethylenediamine. After having stirred the reaction mixture for three hours at −70° C., the reaction mixture was returned to a temperature in the region of 20° C. and the solution obtained was run into a solution of 75 cm3 (0.55 mol) of ethyl oxalate in 110 cm3 of tetrahydrofuran, the temperature being maintained at −75° C., for 1 hour. The reaction mixture was hydrolysed with 800 cm3 of a saturated aqueous sodium hydrogencarbonate solution, extracted with three times 100 cm3 of ethyl acetate, washed with three times 50 cm3 of a normal aqueous hydrochloric acid solution, dried over sodium sulphate and concentrated under reduced pressure. 44 g (97%) of ethyl (RS)-2-oxo-3-phenylbutyrate were then obtained in the form of an orange oil, the characteristics of which were as follows:
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06218406B1 |
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| 出典データセット | uspto-grants-2001_04 |
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| ORD ID | ord-fa29ffcf227e4afca097cbed42620e38 |
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| 出典メモ | uspto-grants-2001_04 |
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