戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 926367作成日:2026年10月25日

Trichloroacetyl chloride → HCID 89733981、化合物

https://huagongshe.com/reaction/926367

反応式

関与物質

役割名称HCID仕込み量
反応物Trichloroacetyl chlorideHCID 6420—
反応物3,4-dihydro-1H-pyrrolo[2,1-c][1,4]oxazine-8-carboxylic acid ((R)-1-phenyl-propyl)-amideHCID 118946037—
溶媒DichloromethaneHCID 6344—
生成物HCID 89733981HCID 8973398176%

反応手順

To a solution of 3,4-dihydro-1H-pyrrolo[2,1-c][1,4]oxazine-8-carboxylic acid ((R)-1-phenyl-propyl)-amide (Comp. No. 9a) (8.5 g, 29.9 mmol) in anhydrous dichloromethane (33 ml) was added trichloro-acetyl chloride (16.3 g, 89.7 mmol). The resulting mixture was stirred overnight at room temperature, after which a second portion of trichloro-acetyl chloride (3 ml) was added. The resulting mixture was stirred for 6 h at 40° C., and then at 25° C. over 2 days, evaporated to dryness. Methyl tert-butyl ether (60 ml) was added and the mixture was stirred. The product precipitated, was filtered off, washed with a small amount of methyl tert-butyl ether and dried in vacuo to give 9.8 g (76%) of 6-(2,2,2-trichloro-acetyl)-3,4-dihydro-1H-pyrrolo[2,1-c][1,4]oxazine-8-carboxylic acid ((R)-1-phenyl-propyl)-amide. LC/MS (method 4): Rt=1.34 min; m/z=429.01 (M+H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09284333B2
出典データセットuspto-grants-2016_03
ORD IDord-5311df023b0b43b7b6f3116ed84edd45
出典メモuspto-grants-2016_03