Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 343542생성일: 2026년 10월 26일
Ethylene Glycol → 4-Cyano-4-(3-cyclopentyloxy-4-methoxyphenyl)-1,1-(ethylenedioxy)cyclohexane
https://huagongshe.com/reaction/343542
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethylene Glycol | HCID 174 | — |
| 반응물 | p-Toluenesulfonic acid | HCID 6101 | — |
| 반응물 | SB-200473 | HCID 9861604 | — |
| 용매 | Benzene | HCID 241 | — |
| 생성물 | 4-Cyano-4-(3-cyclopentyloxy-4-methoxyphenyl)-1,1-(ethylenedioxy)cyclohexane | HCID 15392036 | — |
반응 단계
A solution of 4-cyano-4-(3-cyclopentyloxy-4-methoxyphenyl)cyclohexan-1-one (1.0 g, 3.19 mmol, prepared by the procedures described in PCT applications PCT/US3/01990 (WIPO publication No. WO 93/19748) and PCT application PCT/US93/02325 published as WIPO number WO 93/19750) in benzene (25 mL) was treated with p-toluenesulfonic acid (5 mg) and ethylene glycol (0.18 mL, 3.19 mmol) and was heated to reflux under an argon atmosphere; water was removed from the mixture via a Dean-Stark trap. After 1.5 h, ether (200 mL) was added, the solution was washed with aqueous 5% sodium bicarbonate and brine, was dried (potassium carbonate) and was evaporated to provide a clear colorless oil. 1H NMR(250 MHz, CDCl3) δ 7.0 (m, 2H), 6.85 (d, J=7 Hz, 1H), 4.8 (m, 1H), 4.0 (m, 4H), 3.85 (s, 3H), 1.58-2.20 (m, 16H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05861421 |
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| 출처 데이터셋 | uspto-grants-1999_01 |
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| ORD ID | ord-b07c7758ae464150a99af07ce7bf92e7 |
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| 출처 메모 | uspto-grants-1999_01 |
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