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HRID 420108作成日:2026年10月25日

Trityl chloride → N-(Triphenylmethyl)-D-serine

https://huagongshe.com/reaction/420108

反応式

関与物質

役割名称HCID仕込み量
反応物Trityl chlorideHCID 6456—
反応物HexamethyldisilazaneHCID 13838—
反応物Ammonium ChlorideHCID 25517—
反応物D-SerineHCID 71077—
溶媒MethanolHCID 887—
溶媒DichloromethaneHCID 6344—
溶媒TriethylamineHCID 8471—
生成物N-(Triphenylmethyl)-D-serineHCID 12042811—

反応条件

温度37.5 °C

反応手順

To dichloromethane (400 ml), D-serine (50 g) was added at ambient temperature under nitrogen atmosphere to form a suspension and then hexamethyldisilazane (134.15 ml) was added to the suspension in 10-15 minutes at ambient temperature. Catalytic amount of ammonium chloride (1 gm) was added. The reaction mixture was refluxed at 35-40° C. for 3 hours and then it was cooled to 0° C. To this mixture, a solution of anhydrous methanol (22.83 g) in dichloromethane (50 ml) was added at 0° C. and the mixture was allowed to reach at room temperature. Triethylamine (48.14 g) was slowly added to it at 25-30° C. and then trityl chloride (132.63 g) was added in 3 lots to the mixture at an interval of 10 minutes. The reaction mixture was then stirred for overnight under nitrogen at ambient temperature. After completion of the reaction, methanol (76.12 g) was added at ambient temperature in 10-15 minutes and the solvent was recovered under vacuum at 40-45° C. Toluene (400 ml) and 5% citric acid solution (750 ml) was added to the recovered solid and filtered. The solid product obtained was washed with water (750 ml) and hexanes (200 ml) and then filtered. The filtered solid was washed with toluene (200 ml) and dried to obtain the titled product. Yield=100 gm; Mass: (-EI): 346 (M−1); 242.9 (-Tr).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08093426B2
出典データセットuspto-grants-2012_01
ORD IDord-bda2f543c4394f1b9d0c998cd2678536
出典メモuspto-grants-2012_01