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HRID 54665作成日:2026年10月25日

Triethylamine → Veratryl alcohol

https://huagongshe.com/reaction/54665

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物2,3-DimethoxybenzaldehydeHCID 66581—
反応物2-Amino-1-(3,4-dimethoxyphenyl)ethan-1-ol hydrochlorideHCID 12888909—
反応物HCID 178418435HCID 178418435—
溶媒MethanolHCID 887—
生成物Veratryl alcoholHCID 7118—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05623074
出典データセットuspto-grants-1997_04
ORD IDord-3bcdb4656b234fc0b193760fcf8acf5b
出典メモuspto-grants-1997_04