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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 842280생성일: 2026년 10월 24일

Triethylamine → 2-[(R)-alpha-methoxy-alpha-trifluoromethylphenylacetylamino]-4-(4-octylphenyl)butanol

https://huagongshe.com/ko/reaction/842280

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물(-)-alpha-Methoxy-alpha-(trifluoromethyl)phenylacetyl chlorideHCID 3080792—
반응물2-Amino-4-(4-octylphenyl)butan-1-olHCID 10064206—
용매DichloromethaneHCID 6344—
생성물2-[(R)-alpha-methoxy-alpha-trifluoromethylphenylacetylamino]-4-(4-octylphenyl)butanolHCID 70146436—

반응 단계

2-Amino-4-(4-octylphenyl)butanol (10 mg), N,N-dimethyl-p-aminopyridine (17.5 mg), anhydrous triethylamine (11.4 μl) and anhydrous methylene chloride (1 ml) were mixed and the mixture was stirred under a nitrogen atmosphere at room temperature. Thereto was added (R)-α-methoxy-α-trifluoromethylphenylacetyl chloride (16.8 μl) and the mixture was stirred at room temperature for 10 hours. The reaction mixture was concentrated under reduced pressure and the residue obtained was purified by thin layer chromatography (eluent; chloroform:methanol=9:1) to give the two diastereomer mixtures. Moreover, the mixture was purified by high performance liquid chromatography (eluent; methanol:water=88:12, flow rate; 8.0 ml /minute) to give the subject oily substance (9.8 mg) of 67.8 minutes at retention time and the subject oily substance (9.6 mg) of 71.6 minutes at retention time.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06372800B1
출처 데이터셋uspto-grants-2002_04
ORD IDord-87dd6862c20c4ff9ad6582dd8128191d
출처 메모uspto-grants-2002_04