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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323379Generated: October 30, 2026

Methyl iodide → Methyl 2-(methylsulfanyl)-5-nitrobenzoate

https://huagongshe.com/reaction/323379

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl acetate hexaneHCID 21226206—
Reactant2-(Methylthio)-5-nitrobenzoic acidHCID 23499961—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductMethyl 2-(methylsulfanyl)-5-nitrobenzoateHCID 7164673—

Reaction Steps

Combine 2-methylthio-5-nitrobenzoic acid, (3.2 g, 15 mmol), N,N-diisopropylethylamine (17.0 mL, 100 mmol), and methyl iodide (12.45 mL, 200 mmol) in acetonitrile (50 mL). After 18 hours, dilute the reaction mixture with ethyl acetate, extract with brine, dry the organic layer over MgSO4, filter, and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting with 20% ethyl acetate/hexane to give methyl 2-methylthio-5-nitrobenzoate. Rf=0.58 (silica gel, 30% ethyl acetate/hexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211199B1
Source datasetuspto-grants-2001_04
ORD IDord-97b035ed12f54e9dbdd5202996626fbe
Source noteuspto-grants-2001_04