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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354252Generated: October 31, 2026

Sodium Hydroxide → HCID 86590215, compound

https://huagongshe.com/reaction/354252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant1-(3-Chlorophenyl)ethanoneHCID 14933—
ReactantSodium hydrideHCID 24758—
Reactant2-Chloro-5-(trifluoromethyl)pyridineHCID 92342—
ReactantHydroxyamine hydrochlorideHCID 443297—
SolventMethanolHCID 887—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 86590215HCID 86590215—

Reaction Conditions

Temperature-10 °C

Reaction Steps

A reaction vessel was charged with sodium hydride (as a 60% oil dispersion, 14.4 g, 360 mmol), DME (120 ml) and 2-chloro-5-trifluoromethylpyridine (20 g, 110 mmol) under nitrogen. 3-Chloroacetophenone (15.5 ml, 200 mmol) was added in portions to the mixture which was stirring at −10° C. The mixture was allowed to warm to ambient temperature and then heated to 40-45° C. for 5 hours. Upon completion of the reaction, the mixture was cooled to 5° C. and 10% aqueous sodium hydroxide solution (60 ml) was slowly added to the reaction mixture followed by methanol (120 ml) then hydroxylamine hydrochloride (38.2 g, 550 mmol). The mixture was heated to 72° C. for 4 hours then cooled and partitioned between water and ethyl acetate, washed with brine and evaporated under vacuum to dryness. The resulting solid was slurried with cyclohexane (60 ml) and dichloromethane (10 ml) then filtered, washing with further cyclohexane. 17.5 g (53%) of the title compound was collected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06756498B2
Source datasetuspto-grants-2004_06
ORD IDord-75e65ab5700e47cba4b38a3dc49672bc
Source noteuspto-grants-2004_06