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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698351Generated: November 1, 2026

1-Bromo-2-Chloroethane → 1-(Pyridin-4-yl)cyclopropanecarboxylic acid

https://huagongshe.com/reaction/1698351

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-2-ChloroethaneHCID 7849—
Reactant4-Pyridineacetic acidHCID 34228—
CatalystBenzyl triethylammonium chlorideHCID 66133—
SolventSodium HydroxideHCID 14798—
Product1-(Pyridin-4-yl)cyclopropanecarboxylic acidHCID 55267109—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a mixture of pyridin-4-yl-acetic acid (930 mg, 6.0 mmol) and 1-bromo-2-chloroethane (750 mg, 9.0 mmol) in 50% NaOH aq. solution (5 mL) is added benzyltriethylammonium chloride (680 mg, 3 mmol). The solution is heated to 60° C. and stirred at the temperature for 2 hours. After cooling down to rt, the aqueous layer is removed and the organic layer is neutralized with sat. NH4Cl aq. and extracted with Et2O. The combined organic phases are washed with H2O and dried over Na2SO4. Concentration under reduced pressure gives the title compound. The material is used in a next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163773B2
Source datasetuspto-grants-2012_04
ORD IDord-7b3c5e84698a4a1b92e141f58d7adfdd
Source noteuspto-grants-2012_04