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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390344Generated: October 29, 2026

Tert-butyl(4-chloro-2-ethynylphenoxy)acetate → (4-Chloro-2-{[5-(isopropylsulfonyl)-2-methylphenyl]ethynyl}phenoxy)acetic acid

https://huagongshe.com/reaction/2390344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl(4-chloro-2-ethynylphenoxy)acetateHCID 56594381—
Reactant2-Bromo-4-(isopropylsulfonyl)-1-methylbenzeneHCID 58522059—
Product(4-Chloro-2-{[5-(isopropylsulfonyl)-2-methylphenyl]ethynyl}phenoxy)acetic acidHCID 46865973—

Reaction Steps

Following the general method as outlined in Example 37, starting from tert-butyl(4-chloro-2-ethynyl phenoxy)acetate (Intermediate 3) and 2-bromo-4-(isopropylsulfonyl)-1-methylbenzene (Intermediate 64), the title compound was obtained as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273769B2
Source datasetuspto-grants-2012_09
ORD IDord-1d5a963bff6e46bc96efb0b421008a10
Source noteuspto-grants-2012_09