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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10176Generated: October 26, 2026

Water → acetophenone O-[2-((morpholin-4-yl))ethyl]oxime

https://huagongshe.com/reaction/10176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantAcetophenonoximeHCID 69185—
ReactantMorpholine, 4-(2-chloroethyl)-, hydrochloride (1:1)HCID 77210—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTolueneHCID 1140—
Productacetophenone O-[2-((morpholin-4-yl))ethyl]oximeHCID 86594237—

Reaction Conditions

Temperature75 °C

Reaction Steps

To a solution of acetophenone oxime (20 g) in toluene (700 mL) was added subsequently tetrabutylammonium bromide (4.77 g), water (8 mL), 4-(2-chloroethyl)morpholine hydrochloride (30.31 g) and finally 50% sodium hydroxide (aq, 52 mL). The resulting mixture was heated at 75° C. overnight. After cooling to room temperature water was added, to dissolve all the salts, the layers were separated, and the aqueous layer was extracted with toluene. The organic layers were dried (MgSO4), and concentrated in vacuo. The residue was purified by flash chromatography (SiO2, CH2Cl2/MeOH 95/5) to afford acetophenone O-[2-((morpholin-4-yl))ethyl]oxime as an oil. The obtained oil was dissolved in 6M HCl (aq, 500 mL) and heated under reflux for 5 hours and subsequently stirred overnight at room temperature. The mixture was extracted with ether and concentrated in vacuo. The residue was crystallized from ethanol, to afford O-[2-((morpholin-4-yl))ethyl]hydroxylamine dihydrochloride. 24.8 g (77%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094779B2
Source datasetuspto-grants-2006_08
ORD IDord-7cdc52eb0f104415883f65036a3b8c9b
Source noteuspto-grants-2006_08