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Ethanol → Ethyl 4-bromo-3-methylbenzoate

HRID 563698
Notes
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Reaction equation

HRID 563698 reaction equation
[Br:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][C:3]=1[CH3:11].S(Cl)(Cl)=O.[CH3:16][CH2:17]O>>[CH2:16]([O:7][C:6](=[O:8])[C:5]1[CH:9]=[CH:10][C:2]([Br:1])=[C:3]([CH3:11])[CH:4]=1)[CH3:17]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 702EthanolHCID 24386Thionyl Chloride2×HCID 821314-Bromo-3-methylbenzoic acid

Product 1

HCID 21729626Ethyl 4-bromo-3-methylbenzoate

Procedure

To 4-bromo-3-methylbenzoic acid (3 g, 14 mmol) in EtOH (200 mL) was added thionyl chloride (2 mL, 25 mmol), and the reaction was stirred for 10 minutes. Additional thionyl chloride (3 mL, 35 mmol) was added, and the reaction was stirred overnight at 50° C. After cooling to room temperature, the mixture was quenched with the slow addition of powdered Na2CO3, and then filtered and concentrated. The residue was partitioned between EtOAc and H2O, and the organic layer was dried, filtered, and concentrated to give the title compound.

Workup

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
stirring
the reaction was stirred overnight at 50° C
  • customthe mixture was quenched with the slow addition of powdered Na2CO3
  • filtrationfiltered
  • concentrationconcentrated
  • customThe residue was partitioned between EtOAc and H2O
  • customthe organic layer was dried
  • filtrationfiltered
  • concentrationconcentrated
  • Sources & evidence

    ORD record
    ord-aef2c2dc02544837b83e32250d5b87e9
    Source dataset
    uspto-grants-2011_11
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US08067445B2

    Reaction notes

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