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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2191687Generated: November 1, 2026

Hydrochloric Acid → Methyl 4-(benzylthio)-2-(4-fluoroanilino)benzoate

https://huagongshe.com/reaction/2191687

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTolueneHCID 1140—
ReactantBenzyl mercaptanHCID 7509—
ReactantMethyl 2-(4-fluoroanilino)-4-iodobenzoateHCID 57667861—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
ProductMethyl 4-(benzylthio)-2-(4-fluoroanilino)benzoateHCID 57667795—

Reaction Conditions

Temperature80 °C

Reaction Steps

To toluene 4.0 mL suspension of methyl 2-(4-fluoroanilino)-4-iodobenzoate 0.40 g, 1,1′-bis(diphenylphosphino)ferrocene 0.072 g and tris(dibenzylideneacetone)dipalladium(0) 0.050 g were added triethylamine 0.30 mL and phenylmethanethiol 0.15 mL, and it was stirred under argon atmosphere at 80° C. for 2 hours. After the reaction mixture was cooled to room temperature, 1.0 mol/L hydrochloric acid and ethyl acetate were added to it. The organic layer was separated and collected,dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The obtained residue was refined by silica gel column chromatography [Fuji SILYSIA Chemical Ltd., PSQ100B(spherical type), eluent, hexane:ethyl acetate=10:1] to give methyl 4-(benzylthio)-2-(4-fluoroanilino)benzoate 0.36 g of white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08327467B2
Source datasetuspto-grants-2012_12
ORD IDord-cb498fe1674b45dba75bcf21a79098a8
Source noteuspto-grants-2012_12