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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390210Generated: October 29, 2026

Tert-butyl(4-chloro-2-ethynylphenoxy)acetate → Tert-butyl(4-chloro-2-{[2-fluoro-5-(isopropylsulfonyl)phenyl]ethynyl}phenoxy)acetate

https://huagongshe.com/reaction/2390210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl(4-chloro-2-ethynylphenoxy)acetateHCID 56594381—
Reactant{[2-Fluoro-5-(propylsulfonyl)phenyl]ethynyl}trimethyl silaneHCID 58521874—
Reactant2-Bromo-1-fluoro-4-(isopropylsulfonyl)benzeneHCID 58521970—
ProductTert-butyl(4-chloro-2-{[2-fluoro-5-(isopropylsulfonyl)phenyl]ethynyl}phenoxy)acetateHCID 58522040—

Reaction Steps

Following the general method as outlined in Intermediate 107, starting from (4-chloro-2-ethynyl-phenoxy)-acetic acid tert-butyl ester (Intermediate 3) and 2-bromo-1-fluoro-4-(isopropylsulfonyl)benzene (Intermediate 128), the title compound was obtained as a white solid 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-3d74f3c4ec924f389ba109f505a5984d
Source noteuspto-grants-2012_09