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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390213Generated: October 28, 2026

Tert-butyl(4-chloro-2-ethynylphenoxy)acetate → HCID 58522061, compound

https://huagongshe.com/reaction/2390213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl(4-chloro-2-ethynylphenoxy)acetateHCID 56594381—
Reactant{[2-Fluoro-5-(propylsulfonyl)phenyl]ethynyl}trimethyl silaneHCID 58521874—
ReactantHCID 58522058HCID 58522058—
ProductHCID 58522061HCID 5852206199%

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-(2-methyl-propane-1-sulfonyl)-benzene (Intermediate 131), the title compound was obtained as a colorless oil in 99% 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-a5c6a5c9d35a4afcb6058baf8ad60bd3
Source noteuspto-grants-2012_09