戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 5901作成日:2026年10月24日

Acetone → (2-(Benzyloxy)-3-methoxyphenyl)methanol

https://huagongshe.com/ja/reaction/5901

反応式

関与物質

役割名称HCID仕込み量
反応物AcetoneHCID 180—
反応物2-(Benzyloxy)-3-methoxybenzaldehydeHCID 1268087—
反応物Sodium borohydrideHCID 4311764—
溶媒EthanolHCID 702—
生成物(2-(Benzyloxy)-3-methoxyphenyl)methanolHCID 92725086%

反応手順

A solution of 43.00 g (0.18 mole) of 2-benzyloxy-3-methoxy-benzaldehyde of Example 1 in 300 mL of absolute ethanol is treated, with stirring, with 7.56 g (0.20 mole) of sodium borohydride. The temperature rises to 50° C. After one-half hour 10 mL of acetone is added, keeping the temperature at less than 60° C. with cooling. After 15 minutes the volatiles are stripped off at reduced pressure. Ice water (500 mL) is added and the product is extracted into 600 mL of ethyl acetate. The dried (Na2SO4) solution is concentrated. The remaining oil is dissolved in 100 mL of warm ether. Petroleum ether is added to turbidity to give 37.70 g (86% yield) of pure product; mp 58°-60° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05246943
出典データセットuspto-grants-1993_09
ORD IDord-27c222d747194cee97fae27c69eb7117
出典メモuspto-grants-1993_09