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HRID 8409作成日:2026年10月23日

Benzyl Chloride → 1,4-Bis(benzyloxy)-2-butene

https://huagongshe.com/ja/reaction/8409

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl ChlorideHCID 7503—
反応物2-Butene-1,4-diolHCID 8065—
反応物Sodium HydroxideHCID 14798—
触媒Tetrabutylammonium BromideHCID 74236—
生成物1,4-Bis(benzyloxy)-2-buteneHCID 4054109114.5%

反応条件

温度60 °C

反応手順

To 48% aqueous sodium hydroxide (127.8 g) was added tetra-n-butylammonium bromide (3.3 g, 10 mmol). The mixture was heated to 60° C. To the mixture was added 2-butene-1,4-diol (17) (30.0 g, 340 mmol), to which was added dropwise benzyl chloride (94.8 g, 743 mmol) at 80±15° C. The mixture was stirred at the same temperature for 2 hours. The reaction mixture was cooled down, and separated after the addition of water (90 ml). To the organic layer was added sulfuric acidic brine. The solution was neutralized by aqueous sodium hydrogen carbonate, separated, mixed with ethyl acetate and concentrated under reduced pressure to yield the objective (18) (104.5 g, quantitative) as an oil residue.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087764B2
出典データセットuspto-grants-2006_08
ORD IDord-4caad36be5ac4269aa3917d91c05067e
出典メモuspto-grants-2006_08