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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491015Generated: October 30, 2026

4-Bromothiophenol → HCID 10640226, compound

https://huagongshe.com/reaction/491015

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromothiophenolHCID 66049—
Reactanttert-Butyl 2-bromo-2-methylpropionateHCID 90290—
ProductHCID 10640226HCID 1064022680%

Reaction Steps

As above, tert-butyl 2-[4-(2-aminoethyl)phenylthio]-2-methylpropionate was obtained in 86% yield by reacting 4-bromothiophenol (1) as a starting material with tert-butyl 2-bromoisobutyrate to obtain tert-butyl 2-(4-bromophenylthio)-2-methylpropionate (2) in 80% yield, reacting it with N-vinyl phthalimide in presence of palladium catalyst for 24 hours to obtain tert-butyl 2-[4-(2-phthalimidoethenyl)phenylthio]-2-methylpropionate (3) in 84% yield, reducing the resulted compound (3) under Wilkinson catalyst to obtain tert-butyl 2-[4-(2-phthalimidoethyl)phenylthio]-2-methylpropionate (4) in 91% yield and then reacting the resulted compound (4) with hydrazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07528276B2
Source datasetuspto-grants-2009_05
ORD IDord-0527445de36b43edbd9f69d44f96a33a
Source noteuspto-grants-2009_05