Potassium Carbonate → 3-(mercaptomethyl)benzoic acid

HRID 1407948Notes

Reaction equation

HRID 1407948 reaction equation
C([S:4][CH2:5][C:6]1[CH:7]=[C:8]([CH:12]=[CH:13][CH:14]=1)[C:9]([OH:11])=[O:10])(=O)C.C(=O)([O-])[O-].[K+].[K+]>CO.O>[SH:4][CH2:5][C:6]1[CH:7]=[C:8]([CH:12]=[CH:13][CH:14]=1)[C:9]([OH:11])=[O:10]

Participants

5

Conditions

Temperature
60 °C

Procedure

Into a 500-mL round-bottom flask, was placed a solution of 3-(acetylthiomethyl)benzoic acid (16.4 g, 78.10 mmol, 1.00 equiv) in methanol (150 mL), and a solution of potassium carbonate (26.9 g, 194.93 mmol, 2.50 equiv) in water (70 mL). The resulting solution was stirred for 4 h at 60° C. The resulting mixture was concentrated under vacuum. The resulting solution was diluted with 200 mL of water and adjusted to pH 3 with 10% hydrochloric acid. The resulting solution was extracted with 3× (100/20 mL) of ethyl acetate/tetrahydrofuran and the organic layers combined. The resulting mixture was washed with 1×100 mL of brine. The mixture was dried over sodium sulfate and concentrated under vacuum. This resulted in 12 g (91%) of 3-(mercaptomethyl)benzoic acid as a brown solid.

Workup

  1. customInto a 500-mL round-bottom flask, was placed
  2. concentrationThe resulting mixture was concentrated under vacuum
  3. additionThe resulting solution was diluted with 200 mL of water
  4. extractionThe resulting solution was extracted with 3× (100/20 mL) of ethyl acetate/tetrahydrofuran
  5. washThe resulting mixture was washed with 1×100 mL of brine
  6. dry with materialThe mixture was dried over sodium sulfate
  7. concentrationconcentrated under vacuum
  8. customThis resulted in 12 g (91%) of 3-(mercaptomethyl)benzoic acid as a brown solid

Sources & evidence

ORD record
ord-7af24018cd254fb99e0107fb916c3bcf
Source dataset
uspto-grants-2014_12
Patent number
US08916569B2

Reaction notes

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