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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
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-methylbenzene | HCID 816792 | — |
| 反応物 | Monosodium phosphate | HCID 23672064 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Cyclohexane | HCID 8078 | — |
| 生成物 | Methyl 4-p-tolylsulfonyl-4-methyl-3-dimethoxymethylpentanoate | HCID 12850320 | 49.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04642372 |
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| 出典データセット | uspto-grants-1987_02 |
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| ORD ID | ord-47f976d2918344008a7a71679f3e0649 |
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| 出典メモ | uspto-grants-1987_02 |
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