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HRID 7329作成日:2026年10月23日

1,4-Dibromobutane → 3-[(4-Bromobutoxy)methyl]-3-ethyloxetane

https://huagongshe.com/ja/reaction/7329

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-DibromobutaneHCID 8056—
反応物HexaneHCID 8058—
反応物Sodium HydroxideHCID 14798—
反応物Oxt-101HCID 76444—
触媒Tetrabutylammonium BromideHCID 74236—
溶媒WaterHCID 962—
生成物3-[(4-Bromobutoxy)methyl]-3-ethyloxetaneHCID 2198931545%

反応条件

温度80 °C

反応手順

Into a 2 L egg plant type flask were charged 46.3 g (0.40 mol) of 3-hydroxymethyl-3-ethyloxetane (product name: OXT-101 manufactured by Toagosei Co., Ltd.), 250.3 g (1.16 mol) of 1,4-dibromobutane (reagent, manufactured by Tokyo Kasei Kogyo Co., Ltd.), and 275 ml of hexane. 500 ml of a 33% sodium hydroxide aqueous solution containing 2 g of tetra-n-butylammonium bromide (reagent, manufactured by Tokyo Kasei Kogyo Co., Ltd.) was added to the mixture and vigorously stirred for 5 hours. After the mixture was refluxed at a temperature of 80° C. for one hour, 500 ml of deionized water was added thereto so as to separate the mixture into an organic phase and an aqueous phase. The aqueous phase was extracted three times with 160 ml of hexane. After the organic phase and the extracted phase were dried over magnesium sulfate, the solvent was distilled out in a vacuum. The resulting transparent liquid was distilled in a vacuum thereby obtaining 44.5 g (0.18 mol) of 3-[(4-bromobutoxy)methyl]-3-ethyloxetane as a distillate at 109° C./532 Pa (yield: 44%, identified with 1H-NMR).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087273B2
出典データセットuspto-grants-2006_08
ORD IDord-9bdd41d1c9294f7b851c289c0070b4ce
出典メモuspto-grants-2006_08