Acetyl chloride → Methyl 4-Amino-2-chlorobenzoate

HRID 1852682Notes

Reaction equation

HRID 1852682 reaction equation
[C:1](Cl)(=O)C.[NH2:5][C:6]1[CH:14]=[CH:13][C:9]([C:10]([OH:12])=[O:11])=[C:8]([Cl:15])[CH:7]=1>CO>[NH2:5][C:6]1[CH:14]=[CH:13][C:9]([C:10]([O:12][CH3:1])=[O:11])=[C:8]([Cl:15])[CH:7]=1

Participants

4

Reactant 2

HCID 6367Acetyl chlorideHCID 171544-Amino-2-chlorobenzoic acid

Product 1

HCID 11839197Methyl 4-Amino-2-chlorobenzoate

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

Acetyl chloride (35.2 mmol, 2.5 mL) was added dropwise to a stirring solution of 4-amino-2-chloro-benzoic acid 70l (12.9 mmol, 2.22 g) in methanol (50 mL). The mixture was heated at reflux for 18 h, cooled, and concentrated under vacuum. The residue was taken up in EtOAc, washed with saturated aqueous NaHCO3 and brine, dried, and concentrated under vacuum. The crude product was purified by flash column chromatography (silica gel, 30% EtOAc/hexanes) to give compound 70m.

Workup

  1. temperatureThe mixture was heated
  2. temperatureat reflux for 18 h
  3. temperaturecooled
  4. concentrationconcentrated under vacuum
  5. washwashed with saturated aqueous NaHCO3 and brine
  6. customdried
  7. concentrationconcentrated under vacuum
  8. customThe crude product was purified by flash column chromatography (silica gel, 30% EtOAc/hexanes)

Sources & evidence

ORD record
ord-ab456db969ee482ebbbdb3b317d905fb
Source dataset
uspto-grants-2015_02
Patent number
US08962607B2

Reaction notes

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