Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390178Generated: October 30, 2026

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

https://huagongshe.com/reaction/2390178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl(4-cyano-2-ethynylphenoxy)acetateHCID 58522073—
Reactant2-Iodo-1-isopropyl-4-(methylsulfonyl)benzeneHCID 58522095—
ProductTert-butyl(4-cyano-2-{[2-isopropyl-5-(methylsulfonyl)phenyl]ethynyl}phenoxy)acetateHCID 5852186474%

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 2-iodo-1-isopropyl-4-(methylsulfonyl)benzene (Intermediate 91), the title compound was obtained as a brown 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-cd0a75a60c0b45ac88fe49ffec9327fa
Source noteuspto-grants-2012_09