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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2415330Generated: October 25, 2026

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

https://huagongshe.com/reaction/2415330

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 numberUS06818660B2
Source datasetuspto-grants-2004_11
ORD IDord-e9552cc16d474d2880b627a1ebdfadb7
Source noteuspto-grants-2004_11