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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661747Generated: October 26, 2026

p-Fluorotoluene-alpha-thiol → benzyl 3-(4-fluorobenzylthio)-N-phenyl-thioacrylimidate

https://huagongshe.com/reaction/661747

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Fluorotoluene-alpha-thiolHCID 85171—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantBenzyl N-phenylpropynthioimidateHCID 86617334—
SolventChloroformHCID 6212—
Productbenzyl 3-(4-fluorobenzylthio)-N-phenyl-thioacrylimidateHCID 86617333—

Reaction Steps

Benzyl N-phenylpropynthioimidate (0.30 g) and 4-fluorobenzylmercaptan were dissolved to chloroform (15 ml), catalytic amount of potassium t-butoxide was added thereto under ice-cooling and stirred at room temperature for 14 hours. The reaction mixture was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=15:1) to obtain benzyl 3-(4-fluorobenzylthio)-N-phenyl-thioacrylimidate (0.15 g) as light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084644B2
Source datasetuspto-grants-2011_12
ORD IDord-ceb10f6f62264911a8fb5cbfff922df2
Source noteuspto-grants-2011_12