戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 236056作成日:2026年10月27日

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

https://huagongshe.com/reaction/236056

反応式

関与物質

役割名称HCID仕込み量
反応物2-Butenoic acid, 4,4-dimethoxy-, methyl ester, (Z)-HCID 582207—
反応物1-(Isopropylsulfonyl)-4-methylbenzeneHCID 816792—
反応物Monosodium phosphateHCID 23672064—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒CyclohexaneHCID 8078—
生成物Methyl 4-p-tolylsulfonyl-4-methyl-3-dimethoxymethylpentanoateHCID 1285032049.2%

反応条件

温度-70 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04642372
出典データセットuspto-grants-1987_02
ORD IDord-47f976d2918344008a7a71679f3e0649
出典メモuspto-grants-1987_02