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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2295965Generated: October 25, 2026

Hydroxylamine → alpha-Phenylbenzoin oxime

https://huagongshe.com/reaction/2295965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxylamineHCID 787—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium AcetateHCID 517045—
ReactantPhenylbenzoinHCID 19793701—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Productalpha-Phenylbenzoin oximeHCID 7399805740%

Reaction Steps

180 g (0.625 mol) of phenylbenzoin was added to a 3 liter, one necked, round bottomed flask fitted with a reflux condenser and a nitrogen bypass. 1.45 liters of methanol was added to dissolve the phenylbenzoin and free hydroxylamine was prepared by treating 177.9 g. (2.56 moles) hydroxylamine hydrochloride with 209.9 g (2.56 moles) of sodium acetate in water. The result solution was added to the phenylbenzoin and the reaction mixtur was stirred for 48 hours at reflux at which time an additional 1.24 moles of hydroxylamine was added. The solution was cooled and filtered. The solids were then placed in a Soxhlet extracted and treated with refluxing hexane. After 72 hours the solid remaining in the extraction thimble was collected to yield 40% of the theoretical yield of pure alpha-phenylbenzoin oxime, m.p. 150°-52° C. (lit. 153.5). The hexane extract can be concentrated yield unreacted phenylbenzoin (50% of theory) which may be recycled to afford additional phenylbenzoin oxime. This material was employed to polymerize 2,6 -xylenol using the following composition:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04427594
Source datasetuspto-grants-1984_01
ORD IDord-0c075adba5a34f31b0eadffc69001a52
Source noteuspto-grants-1984_01