돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 31739생성일: 2026년 10월 23일

Trifluoroacetic acid → 4-acetyl-N-(3-methoxybenzyl)benzamide

https://huagongshe.com/ko/reaction/31739

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물4-MethylmorpholineHCID 7972—
반응물4-Acetylbenzoic AcidHCID 11470—
반응물3-MethoxybenzylamineHCID 21156—
반응물PyBOPHCID 2724699—
용매DichloromethaneHCID 6344—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물4-acetyl-N-(3-methoxybenzyl)benzamideHCID 5984089597%

반응 단계

The Sasrin resin was prepared as described in Step 2 of Example 3. The resin (500 mg) was heated with a solution of 3-methoxybenzylamine (600 μl ) in NMP (6 ml) at 70° C. for 4 hours. The resin was then washed with DMF and dichloromethane and then shaken with a solution of PyBop® (1.04 g, 2 mmol), 4-acetylbenzoic acid (0.33 g, 2 mmol), 4-methylmorpholine (4 mmol) in NMP (6 ml) at room temperature overnight. A small aliquot of the resin was treated with 20% TFA in dichloromethane to give the intermediate, (4-acetylphenyl)-N-[(3-methoxyphenyl)methyl]carboxamide (HPLC: 23.94 min (97%); MS; MH+=284 (as required)). The resin was then heated at 95° C. for 7 hours in DMFDMA (5 ml).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425557B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-1818aeeacb4c4b8996cc79a60014620c
출처 메모uspto-grants-2008_09