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HRID 440202作成日:2026年10月26日

1,5-Dibromopentane → 5-Bromopentoxymethylstyrene

https://huagongshe.com/reaction/440202

反応式

関与物質

役割名称HCID仕込み量
反応物1,5-DibromopentaneHCID 8100—
反応物Sodium HydroxideHCID 14798—
反応物alpha-Vinylbenzyl alcoholHCID 92986—
反応物1,1-Diphenyl-2-picrylhydrazyl (free radical)HCID 2735032—
触媒Tetrabutylammonium BromideHCID 74236—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物5-BromopentoxymethylstyreneHCID 5417029351%

反応手順

Into 1ι four-necked flask, 57 g (1.425 mol) of sodium hydroxide and 57 ml of deionized water were added under cooling with ice, and a solution of 98.33 g (0.428 mol) of 1,5-dibromopentane and 9.19 g (0.0285 mol) of tetrabutylammonium bromide in 285 mol of toluene was added thereto. The temperature of the solution was set at 50° C., and 70 ml of a toluene solution of 38.25 g (0.285 mol) of vinyl benzyl alcohol (a mixture of m-form and p-form) and 30 mg of DPPH, was dropwise added thereto over a period of one hour. Most of the raw material disappeared during the dropwise addition. This mixture was reacted at 60° C. for 8 hours with vigorous stirring. After the reaction, the organic phase was separated and thoroughly washed with water. This organic phase was dried over magnesium sulfate, and then toluene was distilled off under reduced pressure. The mixture thereby obtained was subjected to vacuum distillation (b.p. 107° to 108° C./40 Pa) in the presence of DPPH to obtain a liquid of a colorless transparent solution. The obtained solution was analyzed by NMR to determine its structure. The amount of 5-bromopentoxymethylstyrene obtained, was 40.8 g, and the yield was 51%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05518627
出典データセットuspto-grants-1996_05
ORD IDord-f37840f7cdfd4ef58d5ef20d94654cda
出典メモuspto-grants-1996_05