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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356917Generated: October 26, 2026

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

https://huagongshe.com/reaction/356917

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 numberUS05840724
Source datasetuspto-grants-1998_11
ORD IDord-ee20706d8f2f4788a12ee24e21de5d84
Source noteuspto-grants-1998_11