Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727265Generated: October 25, 2026

Thiophenol → Methyl 4-(phenylsulfanylmethyl)benzoate

https://huagongshe.com/reaction/1727265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophenolHCID 7969—
ReactantMethyl 4-(bromomethyl)benzoateHCID 256687—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
ProductMethyl 4-(phenylsulfanylmethyl)benzoateHCID 36656681%

Reaction Steps

To a mixture of benzenethiol (1.3 mL, 13.1 mmol) and potassium tert-butoxide (1.47 g, 13.1 mmol) in DMF (50 mL) at 0° C. was added 4-(bromomethyl)benzoic acid methyl ester (3.0 g, 13.1 mmol), and the mixture was stirred at room temperature for 1 hour. After stirring at 80-90° C. overnight, the reaction mixture was evaporated to dryness under reduced pressure. The residue was dissolved in water (30 mL) and extracted with CH2Cl2 (200 mL). The organic layer was dried (MgSO4) and evaporated under reduced pressure. The crude product was purified by MPLC on silica gel (10% EtOAc in hexanes) to afford the titled compound (2.74 g, 81%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495022B2
Source datasetuspto-grants-2009_02
ORD IDord-202461df03124465a16b3108c758693b
Source noteuspto-grants-2009_02