참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Carbon Disulfide | HCID 6348 | — |
| 반응물 | Ethyl chloroformate | HCID 10928 | — |
| 반응물 | 2-(2-Aminoethyl)-1-methylpyrrolidine | HCID 98388 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 2-(2-Isothiocyanatoethyl)-1-methylpyrrolidine | HCID 21992328 | 43.2% |
반응 단계
A mixture of carbon disulfide (0.996 mL, 16.57 mmol) in water (5 mL) was cooled to 0° C. Then 2-(2-aminoethyl)-1-methylpyrrolidine (2.4 mL, 16.57 mmol) was added over 45 minutes. The resulting mixture was maintained at 0° C. for an additional 30 minutes and then the cooling was discontinued. Next, ethyl chloroformate (1.58 mL, 16.57 mmol) was added over a 1 h period. The resulting mixture was maintained at room temperature for an additional 30 minutes and then made basic with saturated sodium hydrogen carbonate in water. The mixture was extracted with diethyl ether (2×50 mL). The extracts were combined, washed with brine (15 mL), dried over anhydrous sodium sulfate, filtered, and concentrated to give a pale yellow oil. The oil was purified by vacuum distillation to give 1.22 g of 2-(2-isothiocyanatoethyl)-1-methylpyrrolidine.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06699866B2 |
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| 출처 데이터셋 | uspto-grants-2004_03 |
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| ORD ID | ord-a3386d6f29e44d2a8fa2b0fb1a07ae9a |
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| 출처 메모 | uspto-grants-2004_03 |
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