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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2089480Generated: October 31, 2026

(E)-4-(4-bromo-2-fluorophenyl)but-3-enoic acid → 4-(4-Bromo-2-fluorophenyl)butanoic acid

https://huagongshe.com/reaction/2089480

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(E)-4-(4-bromo-2-fluorophenyl)but-3-enoic acidHCID 67547376—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product4-(4-Bromo-2-fluorophenyl)butanoic acidHCID 60676607—

Reaction Steps

To a solution of (E)-4-(4-bromo-2-fluoro-phenyl)-but-3-enoic acid (0.730 g, 2.536 mmol) in ethyl acetate (12 mL) is added palladium on carbon (10% wt., 0.270 g, 0.254 mmol) and the flask is flushed with hydrogen. After 16 hours under a H2 atmosphere (balloon pressure), the mixture is filtered, concentrated and then resubmitted to the same conditions. After 6 hours, the mixture is filtered and concentrated to give 4-(4-bromo-2-fluoro-phenyl)-butyric acid, which is used in the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436035B2
Source datasetuspto-grants-2013_05
ORD IDord-3c38211921b74f8bbe26a5585b3c3c4b
Source noteuspto-grants-2013_05