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HRID 336212作成日:2026年10月27日

Hexamethylphosphoramide → (3S,5S,6R)-3-(5-Chloro-pentyl)-2-oxo-5,6-diphenyl-morpholine-4-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/336212

反応式

関与物質

役割名称HCID仕込み量
反応物HexamethylphosphoramideHCID 12679—
反応物1-Chloro-5-iodopentaneHCID 108914—
反応物tert-butyl (2R,3S)-6-oxo-2,3-diphenylmorpholine-4-carboxylateHCID 981230—
反応物Sodium bis(trimethylsilyl)amideHCID 2724254—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物(3S,5S,6R)-3-(5-Chloro-pentyl)-2-oxo-5,6-diphenyl-morpholine-4-carboxylic acid tert-butyl esterHCID 10961504—

反応条件

温度-78 °C

反応手順

A 1.0M solution of sodium bis(trimethylsilyl)amide in THF (55.0 mL, 55.2 mmol) is added at −78° C. to a solution of (5S,6R)-5,6-diphenyl-4-tert-butoxycarbonyl-morpholin-2-one (13.0 g, 36.8 mmol), 1-chloro-5-iodo-pentane (25.0 g, 108.0 mmol) and HMPA (55.0 mL) in THF (200.0 mL). The reaction mixture is stirred at −78° C. for 2 hours and at room temperature for 1 hour. The reaction mixture is diluted with EtOAc, washed with water and brine. After drying the organic phase over anhydrous Na2SO4, the solvent is removed under reduced pressure to afford the crude product that is purified by silica gel column chromatography to afford the title compound; m/z 358 [M-Boc+H].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08889670B2
出典データセットuspto-grants-2014_11
ORD IDord-a314b8452555435e9290bcb694219f81
出典メモuspto-grants-2014_11