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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7799생성일: 2026년 10월 23일

Hydrochloric Acid → 4-Benzyloxy-1-butanol

https://huagongshe.com/ko/reaction/7799

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Benzyl BromideHCID 7498—
반응물1,4-ButanediolHCID 8064—
반응물Sodium hydrideHCID 24758—
용매TetrahydrofuranHCID 8028—
생성물4-Benzyloxy-1-butanolHCID 56221248%

반응 단계

While a suspension containing 2.5 g of 60% sodium hydride was in 50 ml of tetrahydrofuran was allowed to stand at room temperature, 5.7 g of 1,4-butanediol was slowly added dropwise thereto. Then, a solution containing 7.5 ml of benzyl bromide in 20 ml of tetrahydrofuran was added dropwise to the reaction mixture at room temperature, followed by stirring at the same temperature for 2 hours. After the addition of a 10% aqueous solution of HCl, the reaction mixture was extracted with diethyl ether. After the organic layer was washed with an aqueous solution of sodium hydrogen carbonate and dried over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure. The resulting residue was purified by silica gel column chromatography using 150 g of silica gel [with an elution solvent comprising hexane-ethyl acetate (4:1)]. Thus, 5.5 g (48% yield) of the title compound was obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087624B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-d83ebcba062b4203a4c9b1278b2181ca
출처 메모uspto-grants-2006_08