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HRID 236056Erstellt: 25. Oktober 2026

2-Butenoic acid, 4,4-dimethoxy-, methyl ester, (Z)- → Methyl 4-p-tolylsulfonyl-4-methyl-3-dimethoxymethylpentanoate

https://huagongshe.com/reaction/236056

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Butenoic acid, 4,4-dimethoxy-, methyl ester, (Z)-HCID 582207—
Edukt1-(Isopropylsulfonyl)-4-methylbenzeneHCID 816792—
EduktMonosodium phosphateHCID 23672064—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelCyclohexaneHCID 8078—
ProduktMethyl 4-p-tolylsulfonyl-4-methyl-3-dimethoxymethylpentanoateHCID 1285032049,2%

Reaktionsbedingungen

Temperatur-70 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04642372
Quelldatensatzuspto-grants-1987_02
ORD IDord-47f976d2918344008a7a71679f3e0649
Quellennotizuspto-grants-1987_02