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

HRID 1646333Notes

Reaction equation

HRID 1646333 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,3 H, CH3), 3.9 (2s,6 H, 2×OCH3), 7.1 (d,1 H), 7.5 (m,2 H).

Workup

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

Sources & evidence

ORD record
ord-91e0581e0770436fa7ea039136433abf
Source dataset
uspto-grants-1993_01
Patent number
US05179112

Reaction notes

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