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HRID 427749作成日:2026年10月25日

2-(Benzyloxy)-5-bromobenzaldehyde → (2-(Benzyloxy)-5-bromophenyl)methanol

https://huagongshe.com/reaction/427749

反応式

関与物質

役割名称HCID仕込み量
反応物2-(Benzyloxy)-5-bromobenzaldehydeHCID 733087—
反応物Sodium borohydrideHCID 4311764—
溶媒EthanolHCID 702—
生成物(2-(Benzyloxy)-5-bromophenyl)methanolHCID 897136—

反応手順

A suspension of 2-benzyloxy-5-bromobenzaldehyde (14.5 g, 50.2 mmol) in absolute ethanol (250 ml) was treated with sodium borohydride (2.6 g, 68.8 mmol). The reaction was stirred and the temperature slowly rose to 33° C. After 1 hour the reaction mixture was evaporated and the residue dissolved in ethyl acetate and poured into a mixture of ice water (200 ml) and 1N HCl (25 ml). The organic layer was separated, washed with aqueous sodium hydrogen carbonate, brine, dried (Na2SO4) and evaporated to give 2-benzyloxy-5-bromobenzyl alcohol as a pale yellow oil (14.85 g, quantitative).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06313148B1
出典データセットuspto-grants-2001_11
ORD IDord-325e740b45744e5babf8867b57e39f40
出典メモuspto-grants-2001_11