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HRID 636264作成日:2026年10月26日

Bromide ion → 4-Pentenenitrile

https://huagongshe.com/reaction/636264

反応式

関与物質

役割名称HCID仕込み量
反応物Bromide ionHCID 259—
反応物Sodium CyanideHCID 8929—
反応物Homoallyl bromideHCID 21241—
反応物1-Bromobut-1-eneHCID 35945—
反応物BromocyclobutaneHCID 78110—
反応物BromomethylcyclopropaneHCID 81503—
溶媒WaterHCID 962—
生成物4-PentenenitrileHCID 11604—
生成物CyclopropylacetonitrileHCID 643447—

反応条件

温度45 °C

反応手順

A flask was equipped with stirrer, reflux condenser, thermometer, and charged with 75 ml of water and 36.8 grams (0.75 mole) sodium cyanide. Stirring was commenced and there was added 8.5 grams of tricapryl(methyl)ammonium chloride (ALIQUAT 336 phase-transfer catalyst) followed by 67.5 grams (0.50 mole) of the bromide product mixture comprising 55.7% cyclopropylmethyl bromide, 37.2% bromocyclobutane, and 7.1% bromobutene. The mixture slowly exothermed to about 50° C. After about 1 hour, heating was commenced so as to maintain the temperature of the mixture at 45° C. After 7 hours, gas chromatographic analysis of the organic phase indicated that cyclopropylmethyl bromide and 4-bromo-1-butene (i.e., bromobutene) were consumed, that cyclobutyl bromide was unchanged, and that cyclopropylacetonitrile and 1-cyano-3-butene were formed. The ratio (area %) of cyclopropylacetonitrile to 1-cyano-3-butene was 88:12. A minute trace (less than 1 area %) of cyanocyclobutane was detected.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06191300B1
出典データセットuspto-grants-2001_02
ORD IDord-988db9ccdd2a4ecd8f7f2c6b747c687f
出典メモuspto-grants-2001_02