関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methanesulfonic Acid | HCID 6395 | — |
| 反応物 | Trifluoroacetic anhydride | HCID 9845 | — |
| 反応物 | Ethyl-4-beta-carboxyethylthio-2-methyl-1,3-cyclohexadiene-1-carboxylate | HCID 11043831 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | Ethyl 5-methyl-4-oxo-2,3,7,8-tetrahydro-4H-1-benzothiopyran-6-carboxylate | HCID 10868786 | 79.5% |
反応手順
A mixture of ethyl-4-β-carboxyethylthio-2-methyl-1,3-cyclohexadiene-1-carboxylate (121.3 g, 0.449 mole) in toluene is stirred at 20° C., treated sequentially with 5.0 ml methanesulfonic acid and portionwise over a 5 minute period with trifluoroacetic anhydride (94.3 g, 0.449 mole) and allowed to stir at ambient temperatures for 18 hours. The resultant reaction mixture is quenched with a 1:1 mixture of ethyl acetate and water and stirred for 15 minutes. The phases are separated. The organic phase is washed with water and concentrated in vacuo to give a residue. Crystallization of the residue from isopropanol/heptane affords the title product as a yellow solid, 90.1 g, (79.5% yield), mp 99°-100° C., identified by 1HNMR and mass spectral analyses.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06008402 |
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| 出典データセット | uspto-grants-1999_12 |
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| ORD ID | ord-018684c72cea4fbf84c379506e2e8857 |
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| 出典メモ | uspto-grants-1999_12 |
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