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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118332Generated: October 31, 2026

Cyclohexyl bromide → HCID 69119835, compound

https://huagongshe.com/reaction/2118332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexyl bromideHCID 7960—
ReactantPotassium CarbonateHCID 11430—
Reactantm-BromobenzenethiolHCID 80597—
SolventDimethylformamideHCID 6228—
ProductHCID 69119835HCID 6911983554.3%

Reaction Steps

To a stirred solution of 3-bromobenzenethiol (5.00 g) in DMF (100 ml) was added cyclohexyl bromide (4.31 g) and potassium carbonate (7.31 g). The mixture was stirred at room temperature under nitrogen for 18 h. The reaction mixture was partitioned between 2N HCl and EtOAC. The organic phase was washed with brine and dried (MgSO4). Filtration and removal of the solvent under reduced pressure gave the title compound (3.89 g). Tlc (silica) (4:1 cyclohexane-diethyl ether) Rf=0.90.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442839B2
Source datasetuspto-grants-2008_10
ORD IDord-601da84035e347dba30dbad4dd98c46e
Source noteuspto-grants-2008_10