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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383528Generated: October 31, 2026

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

https://huagongshe.com/reaction/1383528

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 numberUS06255326B1
Source datasetuspto-grants-2001_07
ORD IDord-78f70c6d55654eb4a3cba3ce90b833a7
Source noteuspto-grants-2001_07