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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047478Generated: October 31, 2026

p-Chlorothiophenol → 2-(4-Chloro-phenylsulfanylmethyl)-1,3,4-trifluoro-benzene

https://huagongshe.com/reaction/1047478

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-ChlorothiophenolHCID 7815—
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
Reactant2,3,6-Trifluorobenzyl bromideHCID 519061—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Chloro-phenylsulfanylmethyl)-1,3,4-trifluoro-benzeneHCID 58950098100%

Reaction Steps

2,3,6-Trifluorobenzyl bromide (9.79 g, 43.3 mmol) and 4-chlorothiophenol (6.23 g, 43.3 mmol) were dissolved in 300 mL of THF. Triethylamine (4.59 g, 45.4 mmol) was added. The solution was stirred at room temperature overnight. 300 mL of EtOAc and 300 mL of water were added. The organic layers were washed with 200 mL 1N HCl solution, dried over Na2SO4 and concentrated. The residue was pure product (12.5 g, quant. yield). 1H NMR (CDCl3 400 MHz) δ 7.30 (d, J=8.8 Hz, 2H), 7.24 (d, J=8.8 Hz, 2H), 7.03 (m, 1H), 6.77 (m, 1H), 4.08 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569521B2
Source datasetuspto-grants-2013_10
ORD IDord-bac4f6d79f244821ab812c5f43b4bfa2
Source noteuspto-grants-2013_10