関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Isopropyl chloroformate | HCID 7917 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | p-Toluenesulfonylsemicarbazide | HCID 82602 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 1-p-Toluenesulfonyl-1-Carbisopropoxy-2-Carbamyl Hydrazine | HCID 20385961 | — |
反応手順
The reaction is conducted in a 2 liter reaction flask equipped with thermometer, mechanical stirrer, dropping funnel, and an ice-water bath. 400 ml. water is placed in the flask and cooled to 10° C. Then 73.4 g. (0.6 mole) of isopropyl chloroformate is added. The mixture is stirred at 10° C. as a filtered solution of 114.5 g. (0.5 moles) of p-toluenesulfonyl semicarbazide in a mixture of 36.5 g. (0.55 mole) of KOH in 400 ml. of water is dropped in over the period of an hour, keeping the temperature near 10° C. (A small amount (7.5 g.) of caustic insoluble solid is filtered from the p-toluenesultonyl semicarbazide salt solution). The reaction mixture in the flask is stirred for an additional hour as the temperature is allowed to rise to 25° C. (the cooling bath is removed). A heating mantle is applied and the stirred mixture is warmed to 45° C. The warm mixture is then filtered and the white crystalline product washed with water and dried overnight at 60° C. in a circulating hot air oven. Yield 145 g. (98.4%). m.p. 210°-212° C. A sample is treated with concentrated ammonium hydroxide, washed with water and dried. m.p.=211°-213° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04175200 |
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| 出典データセット | uspto-grants-1979_11 |
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| ORD ID | ord-d54ed9250267474ba28690bd9b62f4b9 |
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| 出典メモ | uspto-grants-1979_11 |
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