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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2275537Generated: November 1, 2026

Ethylene Glycol → 1-[4-(Difluoromethoxy)phenyl]cyclopropanecarboxylic acid

https://huagongshe.com/reaction/2275537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
Reactant1-Bromo-2-ChloroethaneHCID 7849—
ReactantSodium HydroxideHCID 14798—
Reactant2-[4-(Difluoromethoxy)phenyl]acetonitrileHCID 2737018—
CatalystBenzyl triethylammonium chlorideHCID 66133—
Product1-[4-(Difluoromethoxy)phenyl]cyclopropanecarboxylic acidHCID 28937733—

Reaction Conditions

Temperature100 °C

Reaction Steps

Sodium hydroxide [50% aqueous solution (3.20 g)], was added to a mixture of [4-(difluoromethoxy)phenyl]acetonitrile (1.00 g, 5.4 mmol), benzyltriethylammonium chloride (0.10 g, 0.4 mmol) and 1-bromo-2-chloro-ethane (1.58 g, 11.0 mmol) at 50° C. overnight. 1,2-Ethanediol (10.00 mL) was then added to the mixture, and the resulting mixture was heated at 100° C. overnight. The mixture was then poured into ice-water (30 mL) and the resulting mixture was then extracted with ethyl ether (2×10 mL). The aqueous phase was acidified (pH=2) with 1N aqueous HCl solution, and then was extracted with ethyl acetate (4×15 mL). The combined organic phase was washed with brine (10 mL), then dried over Na2SO4, then filtered, and then concentrated under reduced pressure. The residue was the desired product which was directly used in the reaction of next step without furoom temperatureher purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126927B2
Source datasetuspto-grants-2015_09
ORD IDord-3c31d58706ad4172bda3555ca6b07c4b
Source noteuspto-grants-2015_09