Chlorosuccinimide → 2-Amino-5-chloro-3-methylbenzoic acid

HRID 1767065Notes

Reaction equation

HRID 1767065 reaction equation
[NH2:1][C:2]1[C:10]([CH3:11])=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[Cl:12]N1C(=O)CCC1=O>CN(C)C=O>[NH2:1][C:2]1[C:10]([CH3:11])=[CH:9][C:8]([Cl:12])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5]

Participants

4

Conditions

Temperature
100 °C

Procedure

To a solution of 2-amino-3-methylbenzoic acid (Aldrich, 15.0 g, 99.2 mmol) in N,N-dimethylformamide (50 mL) was added N-chlorosuccinimide (13.3 g, 99.2 mmol) and the reaction mixture was heated to 100° C. for 30 minutes. The heat was removed, the reaction was cooled to room temperature and let stand overnight. The reaction mixture was then slowly poured into ice-water (250 mL) to precipitate a white solid. The solid was filtered and washed four times with water and then taken up in ethyl acetate (900 mL). The ethyl acetate solution was dried over magnesium sulfate, evaporated under reduced pressure and the residual solid was washed with ether to afford the desired intermediate as a white solid (13.9 g).

Workup

  1. customThe heat was removed
  2. temperaturethe reaction was cooled to room temperature
  3. additionThe reaction mixture was then slowly poured into ice-water (250 mL)
  4. customto precipitate a white solid
  5. filtrationThe solid was filtered
  6. washwashed four times with water
  7. dry with materialThe ethyl acetate solution was dried over magnesium sulfate
  8. customevaporated under reduced pressure
  9. washthe residual solid was washed with ether

Sources & evidence

ORD record
ord-6e8d5480d7cf43b6b5965fee1b3f2609
Source dataset
uspto-grants-2007_06
Patent number
US07232836B2

Reaction notes

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