Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2180014Generated: November 1, 2026

4-(Bromoacetyl)benzonitrile → HCID 54549064, compound

https://huagongshe.com/reaction/2180014

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Bromoacetyl)benzonitrileHCID 98654—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 53914229HCID 53914229—
SolventAcetonitrileHCID 6342—
ProductHCID 54549064HCID 5454906435%

Reaction Conditions

Temperature0 °C

Reaction Steps

4-Cyanophenacyl bromide (225 mg; 1 mmol) was added to a stirred solution of iso-propyl 3,7-diazabicyclo[3.3.1]nonane-3-carboxylate (from step (iv) above; 212 mg; 1 mmol) in MeCN (2 mL). After stirring for 15 min at 0° C., NaBH4 (40 mg; 1 mmol) was added, and the reaction was allowed to warm to rt over 45 minutes. The reaction mixture was concentrated, dissolved in CH2Cl2 and washed with NaHCO3 (aq.) and brine. The organic layer was separated, dried and concentrated to give an oil which was purified using column chromatography (hexane:EtOAc:IPA; 50:49:1) to give the sub-title compound in 35% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06887881B1
Source datasetuspto-grants-2005_05
ORD IDord-30dc8061ee13496faa248a3e549ea0b0
Source noteuspto-grants-2005_05