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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514692Generated: October 29, 2026

alpha-Chloro-m-nitrotoluene → Methyl(3-nitrobenzyl)sulfane

https://huagongshe.com/reaction/514692

Reaction equation

Participants

RoleNameHCIDCharge
Reactantalpha-Chloro-m-nitrotolueneHCID 12078—
ReactantSodium methanethiolateHCID 4378561—
SolventEthanolHCID 702—
ProductMethyl(3-nitrobenzyl)sulfaneHCID 22031873100.4%

Reaction Steps

Sodium methanethiolate (13.5 g; 192 mmol) was added in two portions to a stirred solution of 1-(chloromethyl)-3-nitrobenzene (30.0 g; 175 mmol) in ethanol (360 mL) at −15° C. The cold bath was removed and the batch was stirred at room temperature for 3 hours. The batch was diluted with brine and extracted with ethyl acetate (2×). The combined organic phases were washed with water, dried (sodium sulfate), filtered and concentrated to give the desired product (32.2 g) that was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108926B2
Source datasetuspto-grants-2015_08
ORD IDord-29cce6b31e0e4c788e331f24e4255fd9
Source noteuspto-grants-2015_08