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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376932Generated: October 25, 2026

Sodium Hydroxide → (R)-2-chloro-6-(oxiran-2-ylmethoxy)benzonitrile

https://huagongshe.com/reaction/376932

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium hydrideHCID 24758—
ReactantBenzenesulfonic acid, 3-nitro-, (2R)-2-oxiranylmethyl esterHCID 146513—
Reactant2-Chloro-6-hydroxybenzonitrileHCID 4407995—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
SolventHexaneHCID 8058—
Product(R)-2-chloro-6-(oxiran-2-ylmethoxy)benzonitrileHCID 44186486—

Reaction Conditions

Temperature0 °C

Reaction Steps

3-Chloro-2-cyanophenol (0.55 g, 3.58 mmol) was dissolved in 10 mL of dimethylformamide, and the solution cooled to 0° C. Sodium hydride (0.158 g, 3.94 mmol 60% in oil), washed with hexane and dimethylformamide, was added to cooled solution over a period of one minute. After stirring for 10 minutes at room temperature, (2R)-(-)-glycidyl 3-nitrobenzenesulfonate was added and stirred 16 hours. The reaction was poured into ether and dilute sodium hydroxide. The ether layer was separated and the aqueous layer extracted once more with ether. The combined ether extracts were washed with water and saturated brine, dried over anhydrous sodium sulfate, filtered, and concentrated to give 0.7 g of (R)-3-chloro-2-cyanophenyl glycidyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06022894
Source datasetuspto-grants-2000_02
ORD IDord-fa80752fd3334d1fa1904cade42ffc2a
Source noteuspto-grants-2000_02