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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 486357생성일: 2026년 10월 25일

Ethylene Glycol → 4-(1,4-Dioxa-8-spiro[4.5]decyl)phenol

https://huagongshe.com/reaction/486357

반응식

참여 물질

역할이름HCID투입량
반응물Ethylene GlycolHCID 174—
반응물HexaneHCID 8058—
반응물HexamethyldisiloxaneHCID 24764—
반응물4-(4'-Hydroxyphenyl)cyclohexanoneHCID 4598916—
용매1,2-DichloroethaneHCID 11—
용매Ethyl AcetateHCID 8857—
생성물4-(1,4-Dioxa-8-spiro[4.5]decyl)phenolHCID 9859480—

반응 단계

A suspension of 13.7 g of 4-(4-hydroxyphenyl)cyclohexanone in 350 ml of ethylene chloride was heated to reflux for 3 hours with 11.6 ml of ethylene glycol and 1.6 g of Amberlyst® 15 (strongly acidic ion exchang resin, Fluka AG) while stirring and separating water. Thereafter, the brown reaction solution was cooled to room temperature and washed twice with 200 ml of water each time. The aqueous phases were backextracted with 200 ml of methylene chloride. The organic phases were dried over sodium sulphate, filtered and concentrated on a rotary evaporator. The brown crystals obtained (17.4 g) were dissolved in 50 ml of hot ethyl acetate. The solution was treated with 50 ml of hexane and left to crystallize in a water bath. The precipitate was filtered off under suction and dried at 50° C., there being obtained 12.4 g of crude product as brown crystals. Working-up of the mother liquor gave a further 4.8 g of crude product. The crude product was purified by chromatography on silica gel with methylene chloride/acetone (volume ratio firstly 97:3, then 95:5) at 0.4 bar. Recrystallization of the orange, crystalline product from ethyl acetate/hexane (vol. 1:2) gave 15.0 g of 4-(1,4-dioxa-8-spiro[4.5]decyl)phenol as yellow-orange crystals with m.p. 151.7°-152.6° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05292452
출처 데이터셋uspto-grants-1994_03
ORD IDord-8893e5a9db814bedb7153941e2e95ba7
출처 메모uspto-grants-1994_03