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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877343Generated: October 29, 2026

3-Hydroxybenzophenone → HCID 71093086, compound

https://huagongshe.com/reaction/877343

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzophenoneHCID 83050—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium AcetateHCID 517045—
ReactantAmmonium AcetateHCID 517165—
CatalystZincHCID 23994—
SolventAmmoniaHCID 222—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
ProductHCID 71093086HCID 71093086—

Reaction Steps

(3-Hydroxyphenyl)(phenyl)methanone (400 g, 2 mol) was dissolved in methanol (4 L). Hydroxylamine hydrochloride (168 g, 2.4 mol) and sodium acetate (331 g, 4 mol) were added to the resulting solution. The mixture was heated at reflux for 18 hours. After cooling to RT solvent was evaporated at reduced pressure, then water (3 L) was added to the residue. The product was extracted with ethyl acetate (3×3 L). The combined organic extracts were washed with saturated aqueous sodium hydrogen carbonate, brine, dried (sodium sulfate), filtered and the solvent evaporated at reduced pressure. The crude residue (1085 g) was used in the next step without purification. The crude oxime, 362 g, (287 g, 1.3 mol of pure oxime based on analysis) was dissolved in ethanol (860 mL) and 25% aqueous ammonia (3000 mL). To this mixture ammonium acetate (52 g, 0.7 mol) was added followed by portion wise addition of zinc powder (440 g, 6.7 mol) to maintain an internal not exceeding 40° C. The mixture was stirred without heating for 18 hours then filtered through a pad of celite. The filter cake was washed with ethyl acetate. The filtrate was collected and the formed layers were separated. The aqueous layer was extracted with ethyl acetate (5×5 L). The combined organic extracts layers were washed with brine (×2) and the solvent was evaporated at reduced pressure. The product was dried in vacuo (35° C., 18 hours).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987299B2
Source datasetuspto-grants-2015_03
ORD IDord-57164a0f26da496796995a9b2e2b938e
Source noteuspto-grants-2015_03