関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sulfuric Acid | HCID 1118 | — |
| 反応物 | Thioglycolic Acid | HCID 1133 | — |
| 反応物 | (4-Aminophenoxy)benzene | HCID 8764 | — |
| 反応物 | Sodium Nitrite | HCID 23668193 | — |
| 触媒 | Copper carbonate | HCID 14452 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | HCID 178526162 | HCID 178526162 | — |
反応手順
4-Phenoxyaniline (30 g, 162 mmol) was added in portions to a stirred solution of 98% w/v sulphuric acid (93 ml) in water (480 ml). The mixture was heated at 80° C. for 30 minutes and then cooled to 0°-5° C. A solution of sodium nitrite (13.5 g, 196 mmol) in water (60 ml) was added dropwise and the mixture was stirred for 45 minutes at 0° C. The excess nitrous acid was destroyed with sulphamic acid. The solution was added to a stirred mixture of 2-mercaptoacetic acid (14.7 ml, 211 mmol), basic copper carbonate (10.8 g, 49 mmol) and acetone (180 ml) at 0° C. The mixture was warmed to ambient temperature. After 1 hour ethyl acetate (200 ml) was added and the insoluble material was removed by filtration. The filtrate was extracted with ethyl acetate. The combined extracts were then extracted with a saturated solution of sodium hydrogen carbonate. The combined aqueous extracts were acidified to pH 2 by the addition of 2M hydrochloric acid and extracted with ethyl acetate. The combined extracts were washed with brine and dried (MgSO4). The solvent was removed by evaporation to give 4-phenoxyphenylthioacetic acid as an oil (12.3 g) having a satisfactory NMR spectrum (200 MHz, CDCl3); 3.61 (s,2H), 6.93-7.46 (m,9 aromatic H), after purification by flash chromatography on silica (Merck Kieselgel Art 9385) using ethyl acetate/dichloromethane (1:1 v/v).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05153227 |
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| 出典データセット | uspto-grants-1992_10 |
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| ORD ID | ord-166f925068d5438c99ba1a38d6e6cbd9 |
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| 出典メモ | uspto-grants-1992_10 |
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