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HRID 1922作成日:2026年10月24日

1,2-Dichloroethane → N-(t-Butoxycarbonyl)-O-Benzyl-D-Serine Allyl Ester

https://huagongshe.com/ja/reaction/1922

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DichloroethaneHCID 11—
反応物Allyl AlcoholHCID 7858—
反応物Ethyl AcetateHCID 8857—
反応物(R)-3-(benzyloxy)-2-((tert-butoxycarbonyl)amino)propanoic acidHCID 2733693—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DichloromethaneHCID 6344—
生成物N-(t-Butoxycarbonyl)-O-Benzyl-D-Serine Allyl EsterHCID 53793486—

反応手順

N-(t-Butoxycarbonyl)-O-benzyl-D-serine (600 mg; 2.03 mmol) was dissolved in dry methylene chloride (5 ml), allyl alcohol (152 μl; 2.23 mmol) and DMAP (25 mg; 0.20 mmol) added and finally EDC (428.5 mg; 2.24 mmol) added to the acid. The reaction mixture was stirred at room temperature for 2.5 h and the resulting homogeneous solution quenched with water and extracted with methylene chloride. The methylene chloride layer was washed with 5% aqueous citric acid then 10% aqueous sodium carbonate solution. The methylene chloride layer was dried over anhydrous magnesium sulfate powder, filtered and evaporated under reduced pressure to give an oil. Chromatography of the oil using ethyl acetate and hexanes 1:2 v/v afforded the product (408 mg; 60%) as a pale yellow gum. FAB-MS:- Calculated for C36H33N5 335.1; found 336.1 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05726319
出典データセットuspto-grants-1998_03
ORD IDord-36f08b8e5c0c4222ab2cf761a8e66449
出典メモuspto-grants-1998_03