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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantButyl vinyl etherHCID 8108—
ReactantPotassium CarbonateHCID 11430—
Reactant1,3-Bis(diphenylphosphino)propaneHCID 81219—
ReactantMethyl 3-bromo-5-methanesulfonylbenzoateHCID 22101072—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductMethyl 3-acetyl-5-(methylsulfonyl)benzoic acidHCID 68830431416.2%

Reaction Conditions

Temperature122 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07476764B2
Source datasetuspto-grants-2009_01
ORD IDord-cf874909ecf14dec9f8a8c08fd3450dd
Source noteuspto-grants-2009_01