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HRID 48569作成日:2026年10月24日

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/ja/reaction/48569

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Benzeneacetic acid, alpha-bromo-, methyl esterHCID 137806—
反応物Isoquinoline, 1-((3,4-dimethoxyphenyl)methyl)-1,2,3,4-tetrahydro-6,7-dimethoxy-, hydrochloride (1:1)HCID 16667431—
反応物Ethyl acetate hexaneHCID 21226206—
溶媒TolueneHCID 1140—
溶媒DichloromethaneHCID 6344—
生成物1-[(3,4-Dimethoxy-benzyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-naphthalen-2-yl]-phenyl-acetic acid methyl esterHCID 6976012591.4%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06703392B2
出典データセットuspto-grants-2004_03
ORD IDord-ea68a220f4284ba196011734ad7e3a3e
出典メモuspto-grants-2004_03