Carbon Disulfide → 2-(2-Isothiocyanatoethyl)-1-methylpyrrolidine

HRID 7811

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HRID 7811 반응식
[C:1](=[S:3])=S.[NH2:4][CH2:5][CH2:6][CH:7]1[CH2:11][CH2:10][CH2:9][N:8]1[CH3:12].ClC(OCC)=O.C(=O)([O-])O.[Na+]>O>[N:4]([CH2:5][CH2:6][CH:7]1[CH2:11][CH2:10][CH2:9][N:8]1[CH3:12])=[C:1]=[S:3]

참가 물질

6

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온도
0 °C

실험 절차

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.

후처리

  1. temperatureThe resulting mixture was maintained at 0° C. for an additional 30 minutes
  2. temperatureThe resulting mixture was maintained at room temperature for an additional 30 minutes
  3. extractionThe mixture was extracted with diethyl ether (2×50 mL)
  4. washwashed with brine (15 mL)
  5. dry with materialdried over anhydrous sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customto give a pale yellow oil
  9. distillationThe oil was purified by vacuum distillation

출처 및 근거

ORD 기록
ord-7e8b147a67fa40c69b7aff3d49bc0289
출처 데이터셋
uspto-grants-2006_08
특허 번호
US07087623B2

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