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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 461734생성일: 2026년 10월 26일

3,4-dihydro-2H-pyran → 2-(p-Bromo-alpha-methylbenzyloxy)tetrahydropyran

https://huagongshe.com/reaction/461734

반응식

참여 물질

역할이름HCID투입량
반응물3,4-dihydro-2H-pyranHCID 8080—
반응물1-(4-Bromophenyl)ethanolHCID 95352—
촉매Hydrochloric AcidHCID 313—
용매Diethyl EtherHCID 3283—
생성물2-(p-Bromo-alpha-methylbenzyloxy)tetrahydropyranHCID 11219861—

반응 조건

온도0 °C

반응 단계

A mixture of 269 parts of p-bromo-α-methylbenzyl alcohol and 225 parts of 2H-3,4-dihydropyran is stirred and cooled to 0° C. Then there are added dropwise 10 drops of concentrated hydrochloric acid solution and the whole is stirred in an ice-bath (room temperature is reached). After stirring for 24 hours, the reaction mixture is poured onto 1200 parts of ether. The organic phase is washed twice with a sodium hydrogen carbonate solution and twice with water, dried, filtered and evaporated. The residue is distilled, yielding 2-(p-bromo-α-methylbenzyloxy)tetrahydropyran; b.p. 165°-177° C. at 20 mm. pressure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04064132
출처 데이터셋uspto-grants-1977_12
ORD IDord-fbaac15cfa1841cd91d91940aa02c778
출처 메모uspto-grants-1977_12