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HRID 987936作成日:2026年10月26日

Hydrochloric Acid → 2-Tert-butoxycarbonylamino-3-(toluene-4-sulfonyloxy)-propionic acid methyl ester

https://huagongshe.com/reaction/987936

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物4-Toluenesulfonyl chlorideHCID 7397—
反応物TriethylamineHCID 8471—
反応物Triethylamine hydrochlorideHCID 11130—
反応物N-Boc-D-serine methyl esterHCID 377723—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物2-Tert-butoxycarbonylamino-3-(toluene-4-sulfonyloxy)-propionic acid methyl esterHCID 281816267.1%

反応条件

温度6 °C

反応手順

A solution of Boc-D-serine methyl ester (9.59 g, 43.8 mmol) in dichloromethane (100 ml) was stirred at −10° C. during the addition of 4-(dimethylamino)pyridine (270 mg, 2.19 mmol), triethylamine hydrochloride (4.19 g, 43.8 mmol) and tosyl chloride (8.35 g, 43.8 mmol). Triethylamine (6.10 ml, 43.8 mmol) was added dropwise at −10° C. over 35 minutes and the resultant slurry was allowed to stand at 6° C. overnight. The reaction mixture was poured into a mixture of ice (35 g), water (35 ml) and 2N hydrochloric acid (20 ml). The aqueous phase was extracted with dichloromethane (35 ml) and the combined organic solutions washed with brine (2*25 ml), dried (anhydrous magnesium sulfate) and concentrated in vacuo to a pale yellow oil. The oil was dissolved in diethyl ether (100 ml) and cooled to 6° C. Once crystallisation started, petrol ether (75 ml) was added in five portions over two hours, and crystallisation was allowed to proceed at 6° C. overnight to give 2-tert-butoxycarbonylamino-3-(toluene-4-sulfonyloxy)-propionic acid methyl ester (10.98 g, 67%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06632826B1
出典データセットuspto-grants-2003_10
ORD IDord-421fe8c6e1644077bac92f1a51c9a832
出典メモuspto-grants-2003_10