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HRID 247462作成日:2026年10月26日

Water → 2-[(7-Methoxy-1,2,3,4-tetrahydronaphth-2-yl)amino]-1-phenylethanol hydrochloride

https://huagongshe.com/reaction/247462

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物PhenylglyoxalHCID 14090—
反応物Sodium borohydrideHCID 4311764—
反応物7-Methoxy-1,2,3,4-tetrahydronaphthalen-2-amine hydrochlorideHCID 14750915—
溶媒MethanolHCID 887—
生成物2-[(7-Methoxy-1,2,3,4-tetrahydronaphth-2-yl)amino]-1-phenylethanol hydrochlorideHCID 2016088520%

反応条件

温度4 °C

反応手順

An amount of 3.53 g of phenylglyoxal is reacted under stirring at room temperature for 3 hours with 5 g of 2-amino-7-methoxy-1,2,3,4-tetrahydronaphthalene hydrochloride in 100 ml of methanol in the presence of 0.9 g of sodium borohydride. After cooling to 4° C., 4,3 g of sodium borohydride are added and the reacting mixture is left under stirring at room temperature for a night. After addition of 20 ml of water, the solution is stirred at room temperature for 15 minutes, then it is evaporated to dryness. The residue is dissolved in 300 ml of ethyl acetate and 60 ml of water; after filtration, the organic phase is separated, dried over magnesium sulfate, filtered and evaporated to dryness. The oil thus obtained is purified by flash-chromatography by using a mixture ethyl acetate/methanol 8/2 as eluant to obtain the 2-[(7-methoxy-1,2,3,4-tetrahydronaphth-2-yl)amino]-1-phenylethanol hydrochloride. Yield: 20% of the theoretical value.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04707497
出典データセットuspto-grants-1987_11
ORD IDord-a395cc8371f745c7a98988b156bd69c4
出典メモuspto-grants-1987_11