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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390169Generated: October 29, 2026

Tert-butyl(4-cyano-2-ethynylphenoxy)acetate → Tert-butyl(2-{[2-chloro-5-(methylsulfonyl)phenyl]ethynyl}-4-cyanophenoxy)acetate

https://huagongshe.com/reaction/2390169

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl(4-cyano-2-ethynylphenoxy)acetateHCID 58522073—
Reactant1-Chloro-2-iodo-4-(methylsulfonyl)benzeneHCID 58522078—
ProductTert-butyl(2-{[2-chloro-5-(methylsulfonyl)phenyl]ethynyl}-4-cyanophenoxy)acetateHCID 5852188674%

Reaction Steps

Following the general method as outlined in Intermediate 79, starting from (4-cyano-2-ethynyl-phenoxy)-acetic acid tert-butyl ester (Intermediate 46) and 1-chloro-2-iodo-4-(methylsulfonyl)benzene (Intermediate 74), the title compound was obtained as a yellow solid in 74% yield after purification by flash column chromatography (silica), eluting with cyclohexane containing increasing amounts of EtOAc.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273769B2
Source datasetuspto-grants-2012_09
ORD IDord-badf037912624951848f6c0819d9aa1a
Source noteuspto-grants-2012_09