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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644694Generated: October 31, 2026

Hydrochloric Acid → 4-(Benzylsulfanyl)benzaldehyde

https://huagongshe.com/reaction/1644694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzyl mercaptanHCID 7509—
ReactantCesium carbonateHCID 10796—
Reactant4-FluorobenzaldehydeHCID 68023—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-(Benzylsulfanyl)benzaldehydeHCID 1284246090%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a stirred mixture of cesium carbonate (12.81 g, 39.33 mmol), benzyl mercaptan (4.7 mL, 39 mmol), and N,N,-dimethylformamide (80 mL) was added 4-fluorobenzaldehyde, slowly over several minutes. The reaction mixture was stirred at 40° C. overnight. The reaction mixture was cooled to room temperature, then diluted with water (500 mL). The resulting mixture was acidified to pH 4 using 1 N aqueous HCl, then extracted with ethyl acetate (3×150 mL). The combined organic layers were washed with water and brine, dried over MgSO4, filtered, and concentrated. A solution of the crude product and dichloromethane was concentrated over silica gel, and the resulting silica gel supported crude product was loaded onto an Analogix SuperFlash™ column. Flash chromatography (100% hexanes -15% ethyl acetate in hexanes) afforded 7.70 g (90%) of 4-(benzylsulfanyl)-benzaldehyde as a slightly pink solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124629B2
Source datasetuspto-grants-2012_02
ORD IDord-2186377eb5b0417fb59f3382efc8300c
Source noteuspto-grants-2012_02