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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1666308생성일: 2026년 10월 26일

1,1'-Carbonyldiimidazole → N-(3-methoxy-benzyl)-N-methyl-2-(3,5-dimetoxyphenyl)-2-(phenylsulfanyl)-acetamide

https://huagongshe.com/reaction/1666308

반응식

참여 물질

역할이름HCID투입량
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물3-Methoxy-N-methylbenzylamineHCID 5152225—
반응물2-(3,5-Dimethoxyphenyl)-2-(phenylsulfanyl)acetic acidHCID 67081798—
용매DichloromethaneHCID 6344—
생성물N-(3-methoxy-benzyl)-N-methyl-2-(3,5-dimetoxyphenyl)-2-(phenylsulfanyl)-acetamideHCID 67081986105.5%

반응 단계

A solution of 2-(3,5-dimethoxyphenyl)-2-(phenyl-sulfanyl)acetic acid (6.0 g) in dichloromethane (50 ml) was treated with 1,1′-carbonyldiimidazole (3.24 g) at room temperature for 2 hours. A solution of N-methyl-3-methoxy-benzylamine (3.4 g) in dichloromethane (15 ml) was added and the stirring was continued for one hour. The reaction mixture was washed with aqueous hydrochloric acid (1M, 50 ml) and aqueous sodium hydroxide (1M, 50 ml). The organic phase was dried and concentrated to dryness leaving crude N-(3-methoxy-benzyl)-N-methyl-2-(3,5-dimetoxyphenyl)-2-(phenylsulfanyl)-acetamide (9.1 g) as a viscous oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08044067B2
출처 데이터셋uspto-grants-2011_10
ORD IDord-370fd67e1c1a41fba3ad8e657cd42e69
출처 메모uspto-grants-2011_10