関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Oxalyl chloride | HCID 65578 | — |
| 反応物 | p-Tetradecyloxyphenylacetic acid | HCID 10472964 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 1-Hydroxy-3-[4-(tetradecyloxy)phenyl]-2-propanone | HCID 20219109 | — |
反応手順
To a suspension of about 60.0 g of (4-tetradecyloxyphenyl)acetic acid in about 400 ml of methylene chloride containing about 0.63 ml of dimethylformamide was added, over about 10 minutes about 27.31 g of oxalyl chloride. After about 2 hours the solvent was removed, the residue was dissolved in hexane and filtered through celite. The solvent was removed and the residue dried in vacuo. An about 110.82 g portion of tris-trimethylsilyloxyethylene was added and the solution was heated at about 95° C., under argon, for about 5 hours. The solution was poured into a mixture of about 30 ml of concentrated hydrochloric acid (about 12N) about 170 ml of water and about 200 ml of tetrahydrofuran with stirring and heat. This mixture was refluxed about 10 minutes, ethyl acetate was added, the warm organic layer separated and washed with brine, saturated sodium bicarbonate solution, then brine, dried and the solvent removed, giving, after recrystallization from hexane, about 52 g of the desired title compound as a white solid, mp. 84°-85° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04640913 |
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| 出典データセット | uspto-grants-1987_02 |
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| ORD ID | ord-4da355b1c1e34f2496e38f104615b413 |
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| 出典メモ | uspto-grants-1987_02 |
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