Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356228Generated: November 2, 2026

Benzyl Bromide → 4-{[4-(Benzyloxy)phenyl]sulfanyl}-2-chlorobenzaldehyde

https://huagongshe.com/reaction/2356228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-4-fluorobenzaldehydeHCID 145024—
Reactant4-MercaptophenolHCID 240147—
SolventDimethylformamideHCID 6228—
Product4-{[4-(Benzyloxy)phenyl]sulfanyl}-2-chlorobenzaldehydeHCID 23094225—

Reaction Conditions

Temperature50 °C

Reaction Steps

p-hydroxythiophenol (2.12 g) was dissolved in N,N-dimethylformamide (40 mL). To this solution, 2-chloro-4-fluorobenzaldehyde (2.66 g) and potassium carbonate (4.64 g) were added and the mixture was stirred for 2 hours at 50° C. Subsequently, benzyl bromide (4.00 mL) was added and the mixture was stirred for 1.5 hours at 50° C. and then for 2.5 hours at 70° C. The reaction mixture was extracted with ethyl acetate and the extract was washed sequentially with water and a saturated aqueous solution of sodium chloride. The organic phase was then dried over anhydrous sodium sulfate. Following addition of water, the solvent was removed by distillation and the residue was purified on a silica gel column chromatography (hexane:ethyl acetate=10:1). This gave the desired product as a colorless solid (5.70 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759326B2
Source datasetuspto-grants-2010_07
ORD IDord-17e1fef26aea433eabd958208aa0e3f3
Source noteuspto-grants-2010_07