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HRID 398025作成日:2026年10月25日

Benzyl Bromide → 4-Benzyloxyphenylacetonitrile

https://huagongshe.com/reaction/398025

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl BromideHCID 7498—
反応物Potassium CarbonateHCID 11430—
反応物4-Hydroxybenzyl cyanideHCID 26548—
溶媒AcetoneHCID 180—
溶媒Ethyl AcetateHCID 8857—
生成物4-BenzyloxyphenylacetonitrileHCID 522804358.3%

反応手順

4-Hydroxybenzyl cyanide (2.5 g, 18.77 mmol), benzyl bromide (3.8 g, 22:5 mmol) and potassium carbonate (45 mmol) were combined in acetone (50 mL) and heated to reflux for 8 h. The reaction was allowed to cool to rt, diluted with ethyl acetate and filtered to remove the solids. The organic layer was concentrated in vacuo to give an oil. The crude benzyl ether was purified by chromatography on silica gel eluting hexane:ethyl acetate (90:10, v:v) to give 4-benzyloxybenzyl cyanide (4.0 g, 95%) which solidified. MS (M+NH4)+=241.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06610731B2
出典データセットuspto-grants-2003_08
ORD IDord-bc2d91ce438746bbbad4db8247c636a0
出典メモuspto-grants-2003_08