Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404683Generated: November 1, 2026

p-Fluoronitrobenzene → 7W-0016

https://huagongshe.com/reaction/1404683

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-FluoronitrobenzeneHCID 9590—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chlorobenzyl mercaptanHCID 580759—
ReactantWater ethylacetateHCID 22728543—
SolventDimethylformamideHCID 6228—
Product7W-0016HCID 148557598%

Reaction Steps

To a solution of 1-fluoro-4-nitrobenzene (1.0 equivalent) and (2-chlorophenyl)methanethiol (1.0 equivalent) in DMF (1.0 M) at rt was added K2CO3 (2.0 equivalents). After 16 h, the rxn was transferred to EtOAc:water (1:1). The organic layer was separated and sequentially washed with water (2×) and brine. The material was dried (MgSO4), filtered and concentrated to afford (2-chlorobenzyl)(4-nitrophenyl)sulfane in 98% yield. The material was taken through without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912336B2
Source datasetuspto-grants-2014_12
ORD IDord-e4c386f426d6471b8e76e81512656e77
Source noteuspto-grants-2014_12