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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470891Generated: October 26, 2026

Ethylene Oxide → 2-Chloro-4-fluoro-3-(2-hydroxyethyl)benzonitrile

https://huagongshe.com/reaction/470891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene OxideHCID 6354—
Reactant2-Chloro-4-fluorobenzonitrileHCID 109000—
ReactantLithium diisopropylamideHCID 2724682—
SolventTetrahydrofuranHCID 8028—
Product2-Chloro-4-fluoro-3-(2-hydroxyethyl)benzonitrileHCID 6700624466.2%

Reaction Steps

To a solution of 2-chloro-4-fluorobenzonitrile (20.0 g, 128.6 mmol) in THF (200 mL) added LDA (28% wt in THF, 71.0 mL, 142.0 mmol) at −78° C. After addition, the mixture was stirred at the same temperature for 5 h, then ethylene oxide (9.7 ml, 194.2 mmol) was added. The reaction mixture was allowed to warm to R. T. gradually and stirred overnight. The reaction was quenched by adding saturated aqueous NH4Cl solution and extracted with EtOAc (400 mL). The EtOAc extracts were washed with water, brine and dried over Na2SO4. After the solvent was removed, the residue was purified by SiO2 column to give 2-chloro-4-fluoro-3-(2-hydroxyethyl)benzonitrile (17.0 g, 66%). 1H NMR (400 MHz, CDCl3, δ in ppm) 7.58 (dd, J=5.5, 8.6 Hz, 1H), 7.10 (t, J=8.6 Hz, 1H), 3.88 (m, 2H), 3.13 (t, J=6.8 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629167B2
Source datasetuspto-grants-2014_01
ORD IDord-982c268836524ff3883871b2400c1d5c
Source noteuspto-grants-2014_01