関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Thioglycolic Acid | HCID 1133 | — |
| 反応物 | Sodium Methoxide | HCID 10942334 | — |
| 反応物 | 2-Chloro-4,5-diphenyloxazole | HCID 13131162 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 4,5-Diphenyl-2-oxazolyl mercaptoacetic acid | HCID 21408360 | — |
反応手順
8.15 g. of the cyclohexyl ester of thioglycolic acid is dissolved in 80 ml. of absolute THF, and 2.6 g. of sodium methylate is added thereto. The reaction mixture is agitated for 15 minutes. Then, 12 g. of 2-chloro-4,5-diphenyl-oxazole (b.p. 170°/0.05 mm.; producible by reacting 4,5-diphenyl-2-oxazolone with POCl3) in 20 ml. of THF is added dropwise. The reaction mixture is refluxed under agitation for 9 hours. The thus-precipitated NaCl is filtered off and the filtrate concentrated by evaporation, thus obtaining the cyclohexyl ester of 4,5-diphenyl-2-oxazolyl-mercaptoacetic acid as an oily residue. The latter 16 g.) is refluxed in 150 ml. of ethanol with 8 g. of pulverized K2CO3 for 2 hours. After conducting the usual working-up operation, 4,5-diphenyl-2-oxazolyl-mercaptoacetic acid is obtained, m.p. 137°-138°.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US03933840 |
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| 出典データセット | uspto-grants-1976_01 |
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| ORD ID | ord-a3af9fe1d3454831988a96387a96a0e4 |
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| 出典メモ | uspto-grants-1976_01 |
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