Methyl chloroformate → 1-Methoxycarbonyl-3-pyrroline

HRID 1061025Notes

Reaction equation

HRID 1061025 reaction equation
[CH2:1]([N:3](CC)[CH2:4][CH3:5])[CH3:2].Cl[C:9]([O:11][CH3:12])=[O:10]>ClCCl.N1CC=CC1>[CH3:12][O:11][C:9]([N:3]1[CH2:4][CH:5]=[CH:2][CH2:1]1)=[O:10]

Participants

5

Procedure

In dichloromethane (20 ml), 3-pyrroline (1.1 ml) was dissolved, followed by the addition of triethylamine (2.6 ml) and methyl chloroformate (1.2 ml) under ice cooling. The resulting mixture was stirred at room temperature for 17 hours. The residue obtained by distilling the reaction mixture under reduced pressure was purified by chromatography on a silica gel column (hexane:ethyl acetate=4:1), whereby the title compound (0.95 g, 52%) was obtained.

Workup

  1. customThe residue obtained
  2. distillationby distilling the reaction mixture under reduced pressure
  3. customwas purified by chromatography on a silica gel column (hexane:ethyl acetate=4:1), whereby the title compound (0.95 g, 52%)
  4. customwas obtained

Sources & evidence

ORD record
ord-bce515c73f684169a12dd1a81c8521c4
Source dataset
uspto-grants-2003_02
Patent number
US06525042B1

Reaction notes

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