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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1970196Generated: November 3, 2026

2-Chlorocyclohexanone → HCID 73799249, compound

https://huagongshe.com/reaction/1970196

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorocyclohexanoneHCID 13203—
ReactantSodium BicarbonateHCID 516892—
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
SolventEthanolHCID 702—
ProductHCID 73799249HCID 73799249—

Reaction Conditions

Temperature22.5 °C

Reaction Steps

3.0 g (22.6 mmol) of 2-chlorocyclohexanone were initially charged in 30 ml of ethanol, and 1.9 g (22.6 mmol) of O-methyl hydroxylamine hydrochloride were added with stirring at from 20 to 25° C. This mixture was stirred for about 20 hours at from 20 to 25° C., adjusted with sat. NaHCO3 solution to a pH between 7 and 8 and extracted with ethyl acetate. After washing with sat. NaCl solution, the combined organic phases were dried and then freed from the solvent. The title compound (3.4 g) was directly used further.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426631B2
Source datasetuspto-grants-2013_04
ORD IDord-2491bd9f249c4fef9226e31ff6c79fa9
Source noteuspto-grants-2013_04