Acetyl chloride → Benzoic acid, 3-methoxy-4-methyl-, methyl ester

HRID 1756363Notes

Reaction equation

HRID 1756363 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:9]=[CH:10][C:11]=1[CH3:12])[C:6]([OH:8])=[O:7].[C:13](Cl)(=O)C>CO>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:9]=[CH:10][C:11]=1[CH3:12])[C:6]([O:8][CH3:13])=[O:7]

Participants

4

Procedure

A solution of 3-methoxy-4-methylbenzoic acid (6.0 g.) in methanol (120 ml.) was treated with acetyl chloride (6 ml.) and stirred for 36 hours. The solution was evaporated. The residue was dissolved in methanol (100 ml.) and the solution evaporated. This procedure was repeated to give methyl 3-methoxy-4-methylbenzoate (6.34 g., 98%) as a colorless oil; NMR: 2.2(s,3H, CH3), 3.9(2s,6H, 2×OCH3), 7.1(d,1H), 7.5 (m,2H).

Workup

  1. customThe solution was evaporated
  2. dissolutionThe residue was dissolved in methanol (100 ml.)
  3. customthe solution evaporated

Sources & evidence

ORD record
ord-ba8de38a147a40a295c8f58985bddc9f
Source dataset
uspto-grants-1995_08
Patent number
US05440035

Reaction notes

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