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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368752Generated: October 30, 2026

Methyl iodide → 4-chloro-2-methyl-5-(methylsulfonyl)Benzoic acid

https://huagongshe.com/reaction/1368752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium SulfiteHCID 24437—
ReactantChlorosulfonic acidHCID 24638—
Reactant4-Chloro-2-methylbenzoic acidHCID 348269—
Product4-chloro-2-methyl-5-(methylsulfonyl)Benzoic acidHCID 10824478—

Reaction Steps

Accordingly, the invention also provides a process for the preparation of N-diaminomethylene-2-methyl-4,5-di(methylsulfonyl)benzamine, characterized in that in the first stage a) according to the invention 2-bromo-5-chlorotoluene is reacted with a secondary or tertiary organolithium compound, particularly preferably sec-butyllithium, and CO2 to give the first intermediate 4-chloro-2-methylbenzoic acid, in stage b) a methylsulfonyl group is introduced by reacting 4-chloro-2-methylbenzoic acid with chlorosulfonic acid, sodium sulfite and methyl iodide to give the corresponding intermediate 2-methyl-4-chloro-5-methylsulfonylbenzoic acid,

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06573404B2
Source datasetuspto-grants-2003_06
ORD IDord-2e39b67b286844e49de78c100a7b1867
Source noteuspto-grants-2003_06