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 | 2-(4-(Acetyloxy)phenyl)acetic acid | HCID 241587 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | Benzeneacetyl chloride, 4-(acetyloxy)- | HCID 182488 | — |
反応手順
250 mg of p-acetoxyphenylacetic acid was dissolved in 5 ml of methylene chloride. To the solution were added, with ice cooling, a catalytic amount of N,N-dimethylformamide and 0.12 ml of oxalyl chloride. The mixture was stirred at room temperature for 1 hour. The reaction mixture was concentrated under reduced pressure to obtain p-acetoxyphenylacetyl chloride. This compound was dissolved in 5 ml of methylene chloride. To the solution was added 260 mg of a sulfur trioxide-dioxane complex with ice cooling. The mixture was stirred at room temperature for 2 hours. The solvent was removed by distillation under reduced pressure to obtain DL-2-(p-acetoxyphenyl)-2-sulfoacetyl chloride. This compound was dissolved in 5 ml of anhydrous tetrahydrofuran.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05300497 |
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| 出典データセット | uspto-grants-1994_04 |
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| ORD ID | ord-8e62da2d1f314fc2909d81dbd7f1711c |
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| 出典メモ | uspto-grants-1994_04 |
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