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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

반응식

참여 물질

역할이름HCID투입량
반응물2-Butenoic acid, 4,4-dimethoxy-, methyl ester, (Z)-HCID 582207—
반응물1-(Isopropylsulfonyl)-4-methylbenzeneHCID 816792—
반응물Monosodium phosphateHCID 23672064—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매CyclohexaneHCID 8078—
생성물Methyl 4-p-tolylsulfonyl-4-methyl-3-dimethoxymethylpentanoateHCID 1285032049.2%

반응 조건

온도-70 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04642372
출처 데이터셋uspto-grants-1987_02
ORD IDord-47f976d2918344008a7a71679f3e0649
출처 메모uspto-grants-1987_02