Methanol → N-Benzylacetamide

HRID 651047Notes

Reaction equation

HRID 651047 reaction equation
[CH2:1]([NH2:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(N(CC)CC)C.[C:16](Cl)(=[O:18])[CH3:17].CO>C(Cl)Cl>[C:16]([NH:8][CH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)(=[O:18])[CH3:17]

Participants

6

Procedure

10 g of benzylamine was dissolved in 200 ml of methylene chloride followed by the addition of 26 ml of triethylamine and dropwise addition of 7.3 ml of acetyl chloride at 0° C. After stirring for 1 hour at room temperature, 2 ml of methanol was added to the reaction system at 0° C. followed by 120 ml of water and separation of the phases. The aqueous layer was extracted with 100 ml of chloroform, and the resulting organic layer was concentrated after drying with anhydrous sodium sulfate to obtain 8.55 g of the target compound (yield: 61%).

Workup

  1. customfollowed by 120 ml of water and separation of the phases
  2. extractionThe aqueous layer was extracted with 100 ml of chloroform
  3. concentrationthe resulting organic layer was concentrated
  4. dry with materialafter drying with anhydrous sodium sulfate

Sources & evidence

ORD record
ord-f8409ae4b1f14e0bb2a3db2ef558e89b
Source dataset
uspto-grants-2001_08
Patent number
US06277859B1

Reaction notes

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