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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647333Generated: October 25, 2026

Hydroxyamine hydrochloride → 1-Acetyl-4-(2-hydroxy-5-methoxybenzoyl)piperidine oxime

https://huagongshe.com/reaction/647333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantAmmonium AcetateHCID 517165—
Reactant1-Acetyl-4-(2-hydroxy-5-methoxybenzoyl)piperidineHCID 13076384—
SolventWaterHCID 962—
Product1-Acetyl-4-(2-hydroxy-5-methoxybenzoyl)piperidine oximeHCID 13640887317.4%

Reaction Steps

A solution of 15.5 g of 1-acetyl-4-(2-hydroxy-5-methoxybenzoyl)-piperidine, 7.0 g of hydroxylamine hydrochloride, 9.5 g of ammonium acetate and 75 ml of water was heated under reflux for 20 hrs. The solution was poured into water and extracted with dichloromethane. The dichloromethane extract was washed with water, dried over anhydrous magnesium sulfate and the solvent was removed in vacuo to give an oil. The oil was triturated with hot toluene. The toluene was decanted and the oil was triturated with ether to give a solid. The tolulene triturant, upon standing, yielded a solid. The solids were combined and recrystallized from acetonitrile to yield 2.8 g (17.4%) of product, mp, 191°-193°, as a mixture of E- and Z-isomers. The chromatogram showed 2 spots.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04408054
Source datasetuspto-grants-1983_10
ORD IDord-d257e2e46fe642f491f80ae86dcb6d44
Source noteuspto-grants-1983_10