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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 48569생성일: 2026년 10월 24일

Triethylamine → 1-[(3,4-Dimethoxy-benzyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-naphthalen-2-yl]-phenyl-acetic acid methyl ester

https://huagongshe.com/ko/reaction/48569

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Benzeneacetic acid, alpha-bromo-, methyl esterHCID 137806—
반응물Isoquinoline, 1-((3,4-dimethoxyphenyl)methyl)-1,2,3,4-tetrahydro-6,7-dimethoxy-, hydrochloride (1:1)HCID 16667431—
반응물Ethyl acetate hexaneHCID 21226206—
용매TolueneHCID 1140—
용매DichloromethaneHCID 6344—
생성물1-[(3,4-Dimethoxy-benzyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-naphthalen-2-yl]-phenyl-acetic acid methyl esterHCID 6976012591.4%

반응 단계

To a white suspension of 1-(4,5-dimethoxybenzyl)6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline-hydrochloride (5 g, 0.013 mol) in dry toluene (50 ml), were added triethylamine (5.5 ml, 0.039 mol) and bromo-phenyl-acetic acid methyl ester (2.07 ml, 0.013 mol). The reaction mixture was stirred at reflux under argon for 20 h. After cooling, the mixture was diluted in CH2Cl2 and washed with water. The aqueous phase was extracted twice with CH2Cl2, the combined organic phases were dried over anhydrous MgSO4, filtered and concentrated to give a crude brown-orange oil. Flash chromatography (AcOEt/hexane 1/1) gave 5.85 g (90%) of the title product as a brown-orange oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06703392B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-ea68a220f4284ba196011734ad7e3a3e
출처 메모uspto-grants-2004_03