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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470212Generated: October 30, 2026

Phenacyl bromide → HCID 86697897, compound

https://huagongshe.com/reaction/470212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
ReactantDiallylamineHCID 31279—
ReactantHydroxyamine hydrochlorideHCID 443297—
CatalystPyridineHCID 1049—
SolventAcetonitrileHCID 6342—
ProductHCID 86697897HCID 8669789779.4%

Reaction Steps

Alpha-bromoacetophenone (77.5 g, 389.36 mmol) is added to a rapidly stirring solution of acetonitrile (1 L) at 0° C. To this solution is added in a drop wise fashion, diallylamine (98.40 mL, 798.18 mmol) over 10 min. The mixture is warmed to room temperature and stirred for 96 h. The solvent is removed under reduced pressure and the residue is dissolved in ethanol (778.71 mL). Pyridine (110.20 mL, 1.36 mmol) is added to the solution followed by hydroxylamine hydrochloride (67.64 g, 973.39 mmol). The reaction is heated to 70° C. for 4 h and then stirred overnight at RT. The solvent is removed under reduced pressure and the residue is dissolved in toluene (1 L). The reaction is heated to 120° C. and stirred overnight. The solvent is removed under reduced pressure. The product is purified via silica gel chromatography eluting with 0-100% ethyl acetate/hexanes to give the title compound as a light red oil (71.2 g, 79.4%) that is used without further purification. EI/MS (m/e): 231.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629270B2
Source datasetuspto-grants-2014_01
ORD IDord-be4c9a482f384f299dbcbb5f2d258f64
Source noteuspto-grants-2014_01