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HRID 7329생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물1,4-DibromobutaneHCID 8056—
반응물HexaneHCID 8058—
반응물Sodium HydroxideHCID 14798—
반응물Oxt-101HCID 76444—
촉매Tetrabutylammonium BromideHCID 74236—
용매WaterHCID 962—
생성물3-[(4-Bromobutoxy)methyl]-3-ethyloxetaneHCID 2198931545%

반응 조건

온도80 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087273B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-9bdd41d1c9294f7b851c289c0070b4ce
출처 메모uspto-grants-2006_08