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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230598Generated: October 26, 2026

Hydrochloric Acid → Methyl 2-methoxy-5-methylsulfinylbenzoate

https://huagongshe.com/reaction/2230598

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
ReactantPhenyltrimethylammonium bromide dibromideHCID 17977687—
ReactantSodium BisulfiteHCID 23665763—
ReactantMethyl 2-methoxy-5-methylthiobenzoateHCID 53727199—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
ProductMethyl 2-methoxy-5-methylsulfinylbenzoateHCID 18464431—

Reaction Steps

Combine methyl 2-methoxy-5-methylthiobenzoate (3.0 g, 14.1 mmol), pyridine (10 mL) and water (10 mL). Cool in an ice bath. Add portionwise phenyltrimethylammonium tribromide (5.84 g, 15.5 mmol). After 30 minutes, warm to ambient temperature. After 3 hour, add a solution of sodium bisulfite (1.6 g) in water (4 mL). After 10 minutes, add a 12 M aqueous hydrochloric acid solution (11 mL) and water. Extract the reaction mixture four times with dichloromethane. Combine the organic layers, extract with brine, dry over Na2SO4, filter, and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting with ethyl acetate to give methyl 2-methoxy-5-methylsulfinylbenzoate: mp; 64-66° C. Elemental Analysis calculated for C9H12O4S: C, 52.62; H, 5.30. Found: C, 52.51; H, 5.:37.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06423704B1
Source datasetuspto-grants-2002_07
ORD IDord-a676c9e2da56444e94c249895842c8fc
Source noteuspto-grants-2002_07