돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1576692생성일: 2026년 10월 25일

Tetrahydrofuran → trans-5,6,7,8-Tetrahydro-1,6,7-naphthalenetriol

https://huagongshe.com/reaction/1576692

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Perchloric AcidHCID 24247—
반응물Sodium BicarbonateHCID 516892—
반응물1a,2,7,7a-Tetrahydronaphtho[2,3-b]oxiren-3-olHCID 12445737—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매ChloroformHCID 6212—
생성물trans-5,6,7,8-Tetrahydro-1,6,7-naphthalenetriolHCID 12445740—

반응 단계

A solution of 8.0 g. (0.048 mole) of 5,6,7,8-tetrahydro-6,7-epoxy-1-naphthol in 100 ml. of tetrahydrofuran is cooled to 0° and 20 ml. of water and 0.5 ml. of 70% perchloric acid are added. After 4 hr., a further 1.5 ml. of acid is added and the solution stirred for 16 hr. at ambient temperature and diluted with 100 ml. each of ether, 10% sodium bicarbonate and saturated salt solution. The aqueous layer is separated and washed with 150 ml. of 1:1 ether-tetrahydrofuran. The organic phase is washed with saturated salt solution, dried and evaporated to give an oil which solidifies on trituration with chloroform. Recrystallization gives in two crops, 4.85 g. of solid which is recrystallized from ethyl acetate to give 3.84 g. m.p. 179.5°-181.5°. Two further recrystallizations of a small sample give the analytical specimen, m.p. 183°-184°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03982021
출처 데이터셋uspto-grants-1976_09
ORD IDord-f0496fda9bca4f0ea323f0a730f12c94
출처 메모uspto-grants-1976_09