Acetic Acid → 3,4-Dihydroxy-5-methoxy-3H-isobenzofuran-1-one

HRID 2297439Notes

Reaction equation

HRID 2297439 reaction equation
C([O:8][C:9]1[C:10]([CH:24]=[O:25])=[C:11]([CH:19]=[CH:20][C:21]=1[O:22][CH3:23])[C:12](N(CC)CC)=[O:13])C1C=CC=CC=1.C(O)(=[O:28])C>Cl>[OH:28][CH:24]1[C:10]2[C:11](=[CH:19][CH:20]=[C:21]([O:22][CH3:23])[C:9]=2[OH:8])[C:12](=[O:13])[O:25]1

Participants

4

Procedure

A solution of 3-benzyloxy-N,N-diethyl-2-formyl-4-methoxy-benzamide (11.6 g, 34 mmoles), prepared as described in example 56, in 10% HCl (80 ml) and acetic acid (80 ml) was refluxed for 18 hours. The solvents were evaporated and the crude taken up in toluene. The solid was washed with ethyl ether and brought to dryness to give 6.66 g of the title compound (quantitative yield) which was used as such in the subsequent step.

Workup

  1. customThe solvents were evaporated
  2. washThe solid was washed with ethyl ether

Sources & evidence

ORD record
ord-ec0d8d5c52fc4ba39ef74c7cff407c16
Source dataset
uspto-grants-2002_12
Patent number
US06492360B1

Reaction notes

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