참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Diethyl Malonate | HCID 7761 | — |
| 반응물 | Magnesium Chloride | HCID 5360315 | — |
| 반응물 | 1,2,3-Benzothiadiazole-7-carbonyl chloride | HCID 18377607 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 용매 | Triethylamine | HCID 8471 | — |
| 생성물 | Diethyl 2-(benzo-1,2,3-thiadiazol-7-yl)malonate | HCID 19793424 | 83.2% |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05248683 |
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| 출처 데이터셋 | uspto-grants-1993_09 |
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| ORD ID | ord-ac19de6fdddf43cb807f1b8ce12dad02 |
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| 출처 메모 | uspto-grants-1993_09 |
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