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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 483753생성일: 2026년 10월 24일

Benzamide → HCID 67754289, 화합물

https://huagongshe.com/ko/reaction/483753

반응식

참여 물질

역할이름HCID투입량
반응물BenzamideHCID 2331—
반응물TriethylamineHCID 8471—
반응물6-Methyl-2-nitrobenzoic acidHCID 16097—
반응물Thionyl ChlorideHCID 24386—
반응물(3S,4R)-4-Amino-2,2-dimethyl-6-(trifluoromethoxy)-chroman-3-olHCID 15020328—
용매BenzeneHCID 241—
용매DichloromethaneHCID 6344—
생성물HCID 67754289HCID 6775428962%

반응 단계

2-Methyl-6-nitrobenzoic acid (1.81 g, 10 mmol) was converted to the corresponding acid chloride by refluxing in benzene (30 mL) with thionyl chloride (1.66 g, 14 mmol) for 0.5 hours. The crude mixture was concentrated in vacuo and diluted with dichloromethane (10 mL). This solution was added to a cooled solution of (3S,4R)-4-amino-2,2-dimethyl-6-(trifluoromethoxy)-chroman-3-ol (2.75 g, 10 mmol), triethylamine (1.39 mL, 10 mmol) and dichloromethane (25 mL). The crude benzamide was worked-up in a method similar to that in Example 1 and chromatographed (1:1 hexanes/ethyl acetate) to afford 2.5 g (62%) of a white solid: m.p. 204°-206° C.; 1H NMR (CDCl3): δ 8.02 (d, 1H), 7.58 (d, 1H), 7.48 (t, 1H), 7.20 (s, 1H), 7.04 (d, 1H), 6.82 (d, 1 H), 6.06 (d, 1H), 3.80 (t, 1H), 3.70 (br s, 1H), 2.56 (s, 3H), 1.52 (s, 3H), 1.31 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05225566
출처 데이터셋uspto-grants-1993_07
ORD IDord-d2add3c02dae4436b92cc53ece9babf4
출처 메모uspto-grants-1993_07