HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1454197Generated: October 27, 2026
Hydrochloric Acid → Methyl 3-acetyl-5-(methylsulfonyl)benzoic acid
https://huagongshe.com/reaction/1454197
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Butyl vinyl ether | HCID 8108 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,3-Bis(diphenylphosphino)propane | HCID 81219 | — |
| Reactant | Methyl 3-bromo-5-methanesulfonylbenzoate | HCID 22101072 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 3-acetyl-5-(methylsulfonyl)benzoic acid | HCID 68830431 | 416.2% |
Reaction Steps
A mixture of methyl 3-bromo-5-(methylsulfonyl)benzoate (66 mg, 0.226 mmol), 1-(vinyloxy)butane (45.3 mg, 0.06 mL, 0.452 mmol), palladium acetate (1.5 mg, 0.0068 mmol), DPPP (6.1 mg, 0.015 mmol) and potassium carbonate (37.5 mg, 0.27 mmol) in DMF (0.6 mL) and H2O (0.07 mL) in a Smith process vial was heated at 122° C. in microwave for 3 h. The reaction mixture was cooled down to room temperature and hydrolyzed by addition of 5% HCl (1 mL) slowly. The reaction mixture was worked up by extraction with ethyl acetate and concentration under vacuum. The crude mixture was purified by reverse phase prep HPLC to give the title compound (16 mg): 1H NMR (CD3OD, 500 MHz) δ ppm 2.74 (3H, s), 3.24 (3H, s), 8.70 (1H, m), 8.75 (1H, m), 8.87 (1H, m). HPLC retention time: 1.037 min (method A). MS (ESI) (M+H)+ 243.10.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07476764B2 |
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| Source dataset | uspto-grants-2009_01 |
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| ORD ID | ord-cf874909ecf14dec9f8a8c08fd3450dd |
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| Source note | uspto-grants-2009_01 |
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