Acetic Anhydride → 5-Methoxy-1,3-dihydro-2-benzofuran-1,3-dione

HRID 334895Notes

Reaction equation

HRID 334895 reaction equation
C(OC(=O)C)(=O)C.[CH3:8][O:9][C:10]1[CH:11]=[C:12]([C:19]([OH:21])=[O:20])[C:13](=[CH:17][CH:18]=1)[C:14]([OH:16])=O>O1CCCC1>[CH3:8][O:9][C:10]1[CH:11]=[C:12]2[C:19](=[O:20])[O:21][C:14](=[O:16])[C:13]2=[CH:17][CH:18]=1

Participants

4

Procedure

Acetic anhydride (40 ml) was added to a mixture of 4-methoxyphthalic acid (30.8 g, 0.16 mol) in anhydrous tetrahydrofuran (150 ml) and the mixture was strirred and held at reflux for 4 hours. Upon cooling to room temperature the solvent was removed in vacuo to afford 4-methoxyphthalic anhydride (27.8 g, 99%) as an off white solid. 1H NMR (DMSO-d6) 8.02 (1H, d), 7.59 (1H, d), 7.49 (1H, dd), 3.97 (3H, s). MS: [M+H]+ 179.

Workup

  1. temperatureat reflux for 4 hours
  2. customwas removed in vacuo

Sources & evidence

ORD record
ord-e62d7be74ad94560835c061646262ff3
Source dataset
uspto-grants-2014_11
Patent number
US08883790B2

Reaction notes

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