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Thionyl Chloride → Methyl 3-chlorocarbonyl-2,4-dichlorobenzoate

HRID 377546
Notes
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Reaction equation

HRID 377546 reaction equation
S(Cl)([Cl:3])=O.[Cl:5][C:6]1[C:15]([C:16](O)=[O:17])=[C:14]([Cl:19])[CH:13]=[CH:12][C:7]=1[C:8]([O:10][CH3:11])=[O:9]>CN(C)C=O.C1(C)C=CC=CC=1>[Cl:3][C:16]([C:15]1[C:6]([Cl:5])=[C:7]([CH:12]=[CH:13][C:14]=1[Cl:19])[C:8]([O:10][CH3:11])=[O:9])=[O:17]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 2

HCID 24386Thionyl ChlorideHCID 18517411Methyl 2,4-dichloro-3-hydroxycarbonylbenzoate

Product 1

HCID 18517406Methyl 3-chlorocarbonyl-2,4-dichlorobenzoateYield 100%

Reagents, catalysts & solvents 2

HCID 6228DimethylformamideCatalystHCID 1140TolueneSolvent

Procedure

Two drops of dimethylformamide and 11.90 g (0.1 mol) of thionyl chloride were added to a solution of 5.00 g (0.02 mol) of methyl 2,4-dichloro-3-hydroxycarbonylbenzoate and 50 ml of dry toluene. The solution was refluxed for 4 hours. After the solvent had been distilled off, 5.35 g of methyl 3-chlorocarbonyl-2,4-dichlorobenzoate were obtained.

Workup

  1. temperatureThe solution was refluxed for 4 hours
  2. distillationAfter the solvent had been distilled off

Sources & evidence

ORD record
ord-93f4750ce6a54134adb0ffd9dc0de74a
Source dataset
uspto-grants-2000_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06028035

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes