Water → N-methoxy-N-methylcyclopentanecarboxamide

HRID 1438370Notes

Reaction equation

HRID 1438370 reaction equation
[CH:1]1([C:6](Cl)=[O:7])[CH2:5][CH2:4][CH2:3][CH2:2]1.CCN(CC)CC.Cl.[CH3:17][NH:18][O:19][CH3:20].O>C(Cl)Cl>[CH3:20][O:19][N:18]([CH3:17])[C:6]([CH:1]1[CH2:5][CH2:4][CH2:3][CH2:2]1)=[O:7]

Participants

6

Procedure

Cyclopentane carbonyl chloride (65 g, 0.49 mol) was added dropwise into a mixture of Et3N (180 mL, 1.3 mol) and N,O-dimethyl hydroxylamine hydrochloride (50 g, 0.52 mol) in anhydrous CH2Cl2 at 0° C. After the addition, the reaction mixture was allowed to stir at ambient temperature overnight. To the reaction mixture was added about 100 g of crushed ice followed 100 g of water. The mixture was separated, and the aqueous layer was extracted with CH2Cl2 (100 mL×2). The combined organic layers were washed with 1N HCl, water, brine and dried over Na2SO4. The solvent was removed under reduced pressure to afford 61 g of desired product as oil in 78.8% of yield.

Workup

  1. additionAfter the addition
  2. customThe mixture was separated
  3. extractionthe aqueous layer was extracted with CH2Cl2 (100 mL×2)
  4. washThe combined organic layers were washed with 1N HCl, water, brine
  5. dry with materialdried over Na2SO4
  6. customThe solvent was removed under reduced pressure

Sources & evidence

ORD record
ord-2cee3957434347928daf7e5f93389384
Source dataset
uspto-grants-2009_11
Patent number
US07622605B2

Reaction notes

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