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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 55838생성일: 2026년 10월 23일

4-Methylmorpholine → N-(2-((tert-butyldimethylsilyloxy)methyl)-4-methoxyphenyl)-3,3,3-trifluoropropanamide

https://huagongshe.com/ko/reaction/55838

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물3,3,3-Trifluoropropionic acidHCID 2777972—
반응물2-((Tert-butyldimethylsilyloxy)methyl)-4-methoxyanilineHCID 66980081—
용매DichloromethaneHCID 6344—
생성물N-(2-((tert-butyldimethylsilyloxy)methyl)-4-methoxyphenyl)-3,3,3-trifluoropropanamideHCID 66980120—

반응 조건

온도20 °C

반응 단계

A mixture of 2-((tert-butyldimethylsilyloxy) methyl)-4-methoxyaniline (14.0 g), 3,3,3-trifluoro-propionic acid (7.30 g, 57.0 mmol), EDCI (15.0 g, 76.5 mmol), HOBT (11.0 g, 80.2 mmol) and NMM (22 mL, 157 mmol) in anhydrous CH2Cl2 (200 mL) was stirred at 20° C. for 2 hours. The mixture was diluted with CH2Cl2 (100 mL), the organic layer was washed with 1M HCl (100 mL), H2O (100 mL) and brine (100 mL), dried over Na2SO4 and concentrated to give the product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09433618B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-773b12b6404c462f850499a2e177f047
출처 메모uspto-grants-2016_09