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HRID 41320作成日:2026年10月24日

Benzaldehyde → 1,2-Diphenylethanol

https://huagongshe.com/ja/reaction/41320

反応式

関与物質

役割名称HCID仕込み量
反応物BenzaldehydeHCID 240—
反応物TetrahydrofuranHCID 8028—
反応物HCID 178419663HCID 178419663—
溶媒Sodium SulfateHCID 24436—
生成物1,2-DiphenylethanolHCID 94178—

反応条件

温度-10 °C

反応手順

To 100 mL (0.10 mol) of 1.0 M BnMgBr in THF 9.50 g (90 mmol) of benzaldehyde (2) was added with vigorous stirring at −10° C. This mixture was slowly warmed to room temperature and then stirred for 2 hr at this temperature. The mixture was added to 300 mL of saturated aqueous Na2SO4. The organic layer was separated and washed with saturated aqueous NH4Cl. The aqueous layer was extracted with 2×100 mL of diethyl ether. The combined organic extracts were evaporated to dryness, and the residue was dissolved in 100 mL of dichloromethane. The obtained solution was dried over Na2SO4 and evaporated to dryness. This crude product was further used without an additional purification. Yield 12.0 g (67%) of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530593B2
出典データセットuspto-grants-2013_09
ORD IDord-a92efe51f65c46a4a278f1dc879cb1d8
出典メモuspto-grants-2013_09