(4-Nitrophenyl)acetic acid → Benzeneacetyl chloride, 4-nitro-

HRID 1988334Notes

Reaction equation

HRID 1988334 reaction equation
[C:1](Cl)(=O)[C:2]([Cl:4])=[O:3].[N+:7]([C:10]1[CH:15]=[CH:14][C:13](CC(O)=O)=[CH:12][CH:11]=1)([O-:9])=[O:8].CN(C=O)C>ClCCl>[N+:7]([C:10]1[CH:15]=[CH:14][C:13]([CH2:1][C:2]([Cl:4])=[O:3])=[CH:12][CH:11]=1)([O-:9])=[O:8]

Participants

5

Reactant 3

HCID 4661(4-Nitrophenyl)acetic acidHCID 6228DimethylformamideHCID 65578Oxalyl chloride

Product 1

HCID 6452210Benzeneacetyl chloride, 4-nitro-

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent2×

Procedure

3.75 ml (7.5 mmoles) of a 2M solution of oxalyl chloride in dichloromethane is added at 20° C. to a solution of 0.9 g (5 mmoles) of 4-nitrophenylacetic acid in a mixture composed of 10 ml of dichloromethane and 0.5 ml of DMF. After agitation for 30 minutes, the solution is concentrated under vacuum. The yellow oil obtained is used without additional purification in the following stage.

Workup

  1. concentrationthe solution is concentrated under vacuum
  2. customThe yellow oil obtained
  3. customis used without additional purification in the following stage

Sources & evidence

ORD record
ord-36d14cacbcd24939befaa1067c2ed7c7
Source dataset
uspto-grants-2009_06
Patent number
US07553976B2

Reaction notes

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