関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Diethyl Malonate | HCID 7761 | — |
| 反応物 | Magnesium Chloride | HCID 5360315 | — |
| 反応物 | 1,2,3-Benzothiadiazole-7-carbonyl chloride | HCID 18377607 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 溶媒 | Triethylamine | HCID 8471 | — |
| 生成物 | Diethyl 2-(benzo-1,2,3-thiadiazol-7-yl)malonate | HCID 19793424 | 83.2% |
反応手順
4.8 g of magnesium chloride in 50 ml of acetonitrile are treated with 7.6 ml of diethyl malonate and 14 ml of triethylamine, with ice-cooling and stirring. The mixture is stirred for 20 minutes and then treated at 0°-5° C. with portions of a suspension of 9.6 g of benzo-1,2,3-thiadiazole-7-carboxylic acid chloride in 50 ml of acetonitrile, the temperature being maintained at between 5° C. and 15° C. The resulting beige suspension is stirred for a further hour in an ice-bath at 0° C. and subsequently overnight at room temperature. On the next day, it is cooled again to 0° C., brought to pH 4.5 using 15% hydrochloric acid, and extracted with ethyl acetate. The extracts are dried over sodium sulfate, filtered over silica gel and evaporated. This results in the title compound in a yield of 83.2% of theory and with a melting point of 72°-74° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05248683 |
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| 出典データセット | uspto-grants-1993_09 |
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| ORD ID | ord-ac19de6fdddf43cb807f1b8ce12dad02 |
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| 出典メモ | uspto-grants-1993_09 |
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