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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 54665생성일: 2026년 10월 23일

Triethylamine → Veratryl alcohol

https://huagongshe.com/ko/reaction/54665

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2,3-DimethoxybenzaldehydeHCID 66581—
반응물2-Amino-1-(3,4-dimethoxyphenyl)ethan-1-ol hydrochlorideHCID 12888909—
반응물HCID 178418435HCID 178418435—
용매MethanolHCID 887—
생성물Veratryl alcoholHCID 7118—

반응 단계

1.0 g of α-(aminomethyl)-3,4-dimethoxybenzyl alcohol hydrochloride was suspended in 5 ml of methanol, and after adding thereto 0.85 g of 2,3-dimethoxybenzaldehyde, 0.63 ml of triethylamine was added dropwise to the mixture while stirring at room temperature. The mixture was heated under reflux for 30 minutes, and 0.24 g of sodium boron hydride was added slowly to the mixture while stirring under ice cooling. After the foaming stopped, the mixture was concentrated. The residue was subjected to a separating procedure with chloroform and water, the chloroform layer was collected, washed with water, and dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was recrystallized from ethyl acetate-n-hexane, giving 1.07 g of α-[[2,3-dimethoxybenzyl)amino]methyl]-3,4-dimethoxybenzyl alcohol, m.p. 96°-97° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05623074
출처 데이터셋uspto-grants-1997_04
ORD IDord-3bcdb4656b234fc0b193760fcf8acf5b
출처 메모uspto-grants-1997_04