Benzene → Acetyl chloride, 2,2'-[1,2-phenylenebis(oxy)]bis-

HRID 1658914Notes

Reaction equation

HRID 1658914 reaction equation
[C:1]([Cl:6])(=[O:5])[C:2](Cl)=[O:3].[CH:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1>>[Cl:6][C:1]([CH2:2][O:3][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[O:3][CH2:2][C:1]([Cl:6])=[O:5])=[O:5]

Participants

3

Reactant 2

HCID 241BenzeneHCID 65578Oxalyl chloride

Product 1

HCID 11076276Acetyl chloride, 2,2'-[1,2-phenylenebis(oxy)]bis-

Procedure

30 g. Of the above acid are added to a mixture of 200 ml. anhydrous benzene. Then 35 g. oxalylchloride are added, the flask being protected by a calcium chloride tube. The mixture is stirred for four days and the diacid progressively dissolves as it is being transformed into the corresponding dichloride. The solution is then evaporated to dryness (without heating) leaving a brownish solid residue which is recrystallized from a mixture of chloroform-benzene giving white crystals.

Workup

  1. additionOf the above acid are added to a mixture of 200 ml
  2. customthe flask being protected by a calcium chloride tube
  3. customThe solution is then evaporated to dryness (without heating)
  4. customleaving a brownish solid residue which
  5. customis recrystallized from a mixture of chloroform-benzene giving white crystals

Sources & evidence

ORD record
ord-e8269324f1e94e6aa493aaf3bff55fa8
Source dataset
uspto-grants-1976_06
Patent number
US03966766

Reaction notes

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