戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1698885作成日:2026年10月27日

1,2-Dichloro-1,1-difluoroethane → N-Boc-S-(2-chloro-1,1-difluoroethyl)-D,L-homocysteine

https://huagongshe.com/reaction/1698885

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-Dichloro-1,1-difluoroethaneHCID 15442—
反応物(tert-Butoxycarbonyl)homocysteineHCID 18322443—
溶媒DimethylformamideHCID 6228—
溶媒Sodium HydroxideHCID 14798—
生成物N-Boc-S-(2-chloro-1,1-difluoroethyl)-D,L-homocysteineHCID 18322437—

反応条件

温度50 °C

反応手順

Ex-18a) A solution of N-Boc-D,L-homocysteine (5 mmol) in NaOH (5 mL, 2N) was slowly added to a stirred solution of 1,2-dichloro-1,1-difluoroethane (5 mmol) in DMF. The resulting solution was then warmed to 50° C. for 16 hours. The reaction solution was then poured onto EtOAc and extracted with citric acid (5%) and brine, dried (Na2SO4) and concentrated in vacuo. The material was purified by flash column chromatography to yield N-Boc-S-(2-chloro-1,1-difluoroethyl)-D,L-homocysteine. Example 18 is prepared in the same manner as described for Example 17 starting with N-Boc-S-(2-chloro-1,1-difluoroethyl)-D,L-homocysteine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06344483B1
出典データセットuspto-grants-2002_02
ORD IDord-150efa6fd236480789542d590f9ef718
出典メモuspto-grants-2002_02