Potassium Carbonate → 3-(mercaptomethyl)benzoic acid
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
Reactant 2
Product 1
Reagents, catalysts & solvents 2
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, dried over sodium sulfate, and concentrated under vacuum. This resulted in 12 g (91%) of 3-(mercaptomethyl)benzoic acid as a brown solid.
Workup
- customInto a 500-mL round-bottom flask, was placed
- concentrationThe resulting mixture was concentrated under vacuum
- additionThe resulting solution was diluted with 200 mL of water
- extractionThe resulting solution was extracted with 3× (100/20 mL) of ethyl acetate/tetrahydrofuran
- washThe resulting mixture was washed with 1×100 mL of brine
- dry with materialdried over sodium sulfate
- concentrationconcentrated under vacuum
- customThis resulted in 12 g (91%) of 3-(mercaptomethyl)benzoic acid as a brown solid
Sources & evidence
- ORD record
- ord-13b8fb9343fe45309d2708d1342dcb4a
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09289430B2
Reaction notes
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