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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807396Generated: October 30, 2026

Acetic Acid → HCID 86669071, compound

https://huagongshe.com/reaction/1807396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 86669072HCID 86669072—
SolventEthanolHCID 702—
ProductHCID 86669071HCID 86669071—

Reaction Steps

A solution of 1-[2-(2,6-dichloro-phenyl)-cyclopropyl]-ethanone O-methyl-oxime (300 mg, 1.16 mmol), prepared as described in example P22, in ethanol (2 ml) and acetic acid (1 ml) was treated at ambient temperature with sodium cyanoborohydride (144 mg, 2.32 mmol) added in one portion. The resulting solution was stirred at ambient temperature for 10 hours. The solvent was evaporated under reduced pressure (co-evaporation with toluene twice) and the residue was slurried with 1 M NaOH (15 ml). The aqueous phase was extracted with ether (3×10 ml), washed with brine and dried over anhydrous Na2SO4. After removal of the solvent, the residue was purified by flash chromatography over silica gel (15 g) (eluent: c-hexane/ethyl acetate 3:1). 260 mg (89.0% of theory) of trans-N-{1-[2-(2,6-dichlorophenyl)-cyclopropyl]-ethyl}-O-methyl-hydroxylamine as a mixture of diastereomeres was obtained in form of a clear liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357635B2
Source datasetuspto-grants-2013_01
ORD IDord-89b5fe98a398434ca330144fcc199ca9
Source noteuspto-grants-2013_01