Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 236056생성일: 2026년 10월 26일
2-Butenoic acid, 4,4-dimethoxy-, methyl ester, (Z)- → Methyl 4-p-tolylsulfonyl-4-methyl-3-dimethoxymethylpentanoate
https://huagongshe.com/reaction/236056
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Butenoic acid, 4,4-dimethoxy-, methyl ester, (Z)- | HCID 582207 | — |
| 반응물 | 1-(Isopropylsulfonyl)-4-methylbenzene | HCID 816792 | — |
| 반응물 | Monosodium phosphate | HCID 23672064 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Cyclohexane | HCID 8078 | — |
| 생성물 | Methyl 4-p-tolylsulfonyl-4-methyl-3-dimethoxymethylpentanoate | HCID 12850320 | 49.2% |
반응 단계
3.4 ml of a 1.95M butyllithium in cyclohexane solution were slowly added at -70° C. to a solution of 1.24 g of p-tolyl isopropyl sulfone in 13 ml of tetrahydrofuran and the mixture was stirred at -70° C. for 15 minutes. Then, a solution of 1 g of methyl 4,4-dimethoxy-2-butenoate in 20 ml of tetrahydrofuran was slowly added to the mixture which was stirred at -70° C. for one hour and poured into a aqueous monosodium phosphate solution. The mixture was extracted with methylene chloride and the organic phase was dried and evaporated to dryness under reduced pressure. The residue was chromatographed over silica gel and was eluted with a 1--1 ether-petroleum ether (b.p.=40°-70° C.) mixture to obtain 1.1 g of methyl 4-p-toluenesulfonyl-4-methyl-3-dimethoxymethyl-pentanoate melting at 110° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04642372 |
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| 출처 데이터셋 | uspto-grants-1987_02 |
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| ORD ID | ord-47f976d2918344008a7a71679f3e0649 |
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| 출처 메모 | uspto-grants-1987_02 |
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