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

HRID 7811

Reaction equation

HRID 7811 reaction equation
[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]

Participants

6

Conditions

Temperature
0 °C

Procedure

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.

Workup

  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

Sources & evidence

ORD record
ord-7e8b147a67fa40c69b7aff3d49bc0289
Source dataset
uspto-grants-2006_08
Patent number
US07087623B2

Linked notes

Loading…