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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489700Generated: October 31, 2026

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

https://huagongshe.com/reaction/1489700

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 numberUS05679696
Source datasetuspto-grants-1997_10
ORD IDord-4a7a5c6f2b3f4611b85f2dd1478e25f3
Source noteuspto-grants-1997_10