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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1826471Generated: November 3, 2026

p-Bromobenzenesulfonyl chloride → 2-Cyclohexyloxyethyl 4-bromobenzenesulfonate

https://huagongshe.com/reaction/1826471

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Bromobenzenesulfonyl chlorideHCID 7396—
Reactant2-Cyclohexyloxy-1-propanolHCID 15218573—
SolventDichloromethaneHCID 6344—
Product2-Cyclohexyloxyethyl 4-bromobenzenesulfonateHCID 2214131380%

Reaction Steps

To a solution of 2-cyclohexyloxy-1-propanol (4.0 g, 28 mmol) in triethylanine (5.8 ml) and dichloromethane (250 ml) was added 4-bromobenzenesulfonyl chloride (7.87 g, 31 mmol) at 0° C. under nitrogen, and the resulting mixture was stirred for 16 h at room temperature. The reaction mixture was washed with saturated aqueous sodium hydrogen carbonate solution, water and brine (100 ml each), dried (MgSO4) and concentrated in vacuo to give the crude product. This was purified by silica (200 g) column chromatography using a gradient elution of hexane:ethyl acetate (6:1 to 1:1) to give the title compound as a white crystalline solid (8.0 g, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07049444B2
Source datasetuspto-grants-2006_05
ORD IDord-94c87038eae94af1a1147548b70b525e
Source noteuspto-grants-2006_05