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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723639Generated: October 30, 2026

Methyl iodide → 2-Chloro-5-(methylsulphonyl)benzoic acid

https://huagongshe.com/reaction/1723639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium HydroxideHCID 14798—
Reactant2-Chloro-5-sulfino-benzoic acidHCID 15112904—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2-Chloro-5-(methylsulphonyl)benzoic acidHCID 2329132—

Reaction Steps

A mixture of 1 g (4 mmol) 2-Chloro-5-sulfino-benzoic acid in 20 ml methanol and 20 ml water was treated with 10N NaOH to pH=9 before adding 1.7 g (12 mmol) methyliodide. The mixture was heated for 48 h to 80° C. with occasional addition of NaOH to maintain pH=9. After removal of all volatiles HCl conc. was added and the mixture was extracted with ethyl acetate. The combined organic layers were dried with MgSO4 and evaporated to dryness. The residue was taken up in methanol and subjected to reversed phase HPLC purification eluting with an acetonitrile/water gradient to yield after evaporation of the product fractions 323 mg (34%) of the title compound. MS (m/e): 233.0 (M−H, 100%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07485637B2
Source datasetuspto-grants-2009_02
ORD IDord-9c18e0ca33194af689794e622c9f4963
Source noteuspto-grants-2009_02