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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 46780생성일: 2026년 10월 23일

Water → 2-(4-Phenoxyphenoxy)cyclopentan-1-ol

https://huagongshe.com/ko/reaction/46780

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium borohydrideHCID 4311764—
반응물3-(4-Phenoxyphenoxy)-cyclopenten-1-eneHCID 20385751—
촉매Mercuric acetateHCID 15337—
용매TetrahydrofuranHCID 8028—
용매Sodium HydroxideHCID 14798—
생성물2-(4-Phenoxyphenoxy)cyclopentan-1-olHCID 22247676—

반응 단계

A solution of 12.6 g of 3-(4-phenoxyphenoxy)-cyclopenten-1-ene in 25 ml of tetrahydrofurane is added dropwise in the course of 1 hour to a mixture of 15.9 g of mercury(II) acetate, 35 ml of water and 50 ml of tetrahydrofurane. The mixture is stirred for about 15 hours at room temperature, then 50 ml of 3 N sodium hydroxide solution are added dropwise in the course of 11/2 hours, followed by the dropwise addition in the course of 1 hour of 50 ml of a 0.5 N solution of sodium borohydride in 3 N sodium hydroxide solution. The reaction mixture is stirred for 2 hours at room temperature and precipitated mercury is removed by filtration. The filtrate is poured into ice-water and, after extraction with ether, the organic phase is washed with saturated sodium chloride solution, dried over sodium sulphate and concentrated by rotary evaporation. Fractional distillation of the residue yields 2-(4-phenoxyphenoxy)cyclopentan-1-ol as a colourless oil with a boiling point of 181°-185° C./0.001 torr.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04175137
출처 데이터셋uspto-grants-1979_11
ORD IDord-68dcc8e1681f4418be9cbbb7c7b244ab
출처 메모uspto-grants-1979_11