関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Carbon Disulfide | HCID 6348 | — |
| 反応物 | Ethyl chloroformate | HCID 10928 | — |
| 反応物 | 2-(2-Aminoethyl)-1-methylpyrrolidine | HCID 98388 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 2-(2-Isothiocyanatoethyl)-1-methylpyrrolidine | HCID 21992328 | 43.2% |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07087623B2 |
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| 出典データセット | uspto-grants-2006_08 |
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| ORD ID | ord-7e8b147a67fa40c69b7aff3d49bc0289 |
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| 出典メモ | uspto-grants-2006_08 |
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