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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230580Generated: October 29, 2026

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

https://huagongshe.com/reaction/2230580

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 numberUS06423704B1
Source datasetuspto-grants-2002_07
ORD IDord-50fb7db24ea84131bbe855b14168c1ba
Source noteuspto-grants-2002_07