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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1870395Generated: November 3, 2026

Methyl 4-chloro-3-nitrobenzoate → Methyl 4-(methylsulfanyl)-3-nitrobenzenecarboxylate

https://huagongshe.com/reaction/1870395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-chloro-3-nitrobenzoateHCID 735797—
ReactantSodium methanethiolateHCID 4378561—
SolventAcetoneHCID 180—
ProductMethyl 4-(methylsulfanyl)-3-nitrobenzenecarboxylateHCID 2118783162.7%

Reaction Steps

A solution of methyl 4-chloro-3-nitrobenzoate (28 g) in acetone (250 mL) is treated portionwise with sodium thiomethoxide (10 g) and the mixture is stirred overnight at room temperature. After filtration, the solution is concentrated and water (300 mL) is added to the residue. The yellow solid is filtered off and subjected to flash chromatography eluting with a mixture of diethyl ether and pentane (1:4 v/v), to give methyl 4-methylthio-3-nitrobenzoate (18.5 g), in the form of a yellow solid, m.p. 118-120° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06096768
Source datasetuspto-grants-2000_08
ORD IDord-5b17a8aa6c884d91b8e5518aa0d6c142
Source noteuspto-grants-2000_08