Hydroquinone → HCID 19816407, compound

HRID 2248059Notes

Reaction equation

HRID 2248059 reaction equation
[C:1]1([CH:8]=[CH:7][C:5]([OH:6])=[CH:4][CH:3]=1)[OH:2].[C:9]([O:12][C:13]1[CH:21]=[CH:20][C:16]([C:17](O)=[O:18])=[CH:15][CH:14]=1)(=[O:11])[CH3:10]>>[C:9]([O:12][C:13]1[CH:21]=[CH:20][C:16]([C:17]([O:2][C:1]2[CH:8]=[CH:7][C:5]([O:6][C:17](=[O:18])[C:16]3[CH:20]=[CH:21][C:13]([O:12][C:9](=[O:11])[CH3:10])=[CH:14][CH:15]=3)=[CH:4][CH:3]=2)=[O:18])=[CH:15][CH:14]=1)(=[O:11])[CH3:10]

Participants

3

Reactant 2

HCID 785HydroquinoneHCID 16865Benzoic acid, 4-(acetyloxy)-

Product 1

HCID 19816407HCID 19816407, compound

Procedure

Using the procedure described above, this compound was prepared from hydroquinone and 4-acetoxybenzoic acid. The crude product was recrystallized from methyl isobutyl ketone (18 ml/g) giving white platelets with a m.p. of 185.0° C. to 186.5° C.

Workup

  1. customThe crude product was recrystallized from methyl isobutyl ketone (18 ml/g)
  2. customgiving white platelets with a m.p. of 185.0° C. to 186.5° C.

Sources & evidence

ORD record
ord-2603ac30f5884c53943dd8eaeed36255
Source dataset
uspto-grants-1991_08
Patent number
US05037938

Reaction notes

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