Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390125Generated: October 25, 2026

3-Bromo-4-fluorobenzyl Alcohol → Tert-butyl(4-chloro-2-{[2-fluoro-5-(hydroxymethyl)phenyl]ethynyl}phenoxy)acetate

https://huagongshe.com/reaction/2390125

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-4-fluorobenzyl AlcoholHCID 2773351—
ReactantTert-butyl(4-chloro-2-ethynylphenoxy)acetateHCID 56594381—
ProductTert-butyl(4-chloro-2-{[2-fluoro-5-(hydroxymethyl)phenyl]ethynyl}phenoxy)acetateHCID 58521982—

Reaction Steps

Following the general method as outlined in Intermediate 19, starting from tert-butyl(4-chloro-2-ethynylphenoxy)acetate (Intermediate 3) and 3-bromo-4-fluorobenzyl alcohol (Oakwood), the title compound was obtained as a dark brown sticky 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-e04f653e86004338931c35289c9c0a8f
Source noteuspto-grants-2012_09