참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethylene Glycol | HCID 174 | — |
| 반응물 | Hexane | HCID 8058 | — |
| 반응물 | Hexamethyldisiloxane | HCID 24764 | — |
| 반응물 | 4-(4'-Hydroxyphenyl)cyclohexanone | HCID 4598916 | — |
| 용매 | 1,2-Dichloroethane | HCID 11 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 4-(1,4-Dioxa-8-spiro[4.5]decyl)phenol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05292452 |
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| 출처 데이터셋 | uspto-grants-1994_03 |
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| ORD ID | ord-8893e5a9db814bedb7153941e2e95ba7 |
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| 출처 메모 | uspto-grants-1994_03 |
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