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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323392Generated: October 25, 2026

Hydrochloric Acid → Methyl 2-methoxy-5-methylsulfinylbenzoate

https://huagongshe.com/reaction/323392

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 numberUS06211199B1
Source datasetuspto-grants-2001_04
ORD IDord-94b1198f11fe470e95e154c23c4c7cdf
Source noteuspto-grants-2001_04