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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566467Generated: October 31, 2026

4-(Bromoacetyl)benzonitrile → HCID 18707465, compound

https://huagongshe.com/reaction/566467

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Bromoacetyl)benzonitrileHCID 98654—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantHCID 21266561HCID 21266561—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18707465HCID 1870746593.8%

Reaction Conditions

Temperature40 °C

Reaction Steps

Potassium bis-(trimethylsilyl)amide (286 mg, 1.43 mMol) was dissolved in anhydrous THF (20 mL) under an atmosphere of dry N2. The mixture was cooled to 40° C. and then 5-(2-hydroxy-ethyl)-5-pyridin-4-ylmethyl-2-thioxo-3-((+)-(2,6,6-trimethyl-bicyclo[3.1.1]-hept-3-ylmethyl))-imidazolidin-4-one (548 mg, 1.37 mMol) was added. The mixture was warmed to ambient temperature and 4-cyanophenacyl bromide (350 mg, 1.43 mMol) was added. The reaction mixture was stirred for one hour after which time it was partitioned between CH2Cl2 and saturated aqueous NaHCO3 solution. The CH2Cl2 layer was dried over Na2SO4, filtered and concentrated under vacuum to give a red foam. The foam was chromatographed on flash silica gel eluting with EtOAc-hexanes (50:50 ) to give 700 mg of the titled compound as a yellow foam as a 1:1 mixture of diastereomers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06174903B1
Source datasetuspto-grants-2001_01
ORD IDord-8cb07e8b13f1472188352fb0070990e8
Source noteuspto-grants-2001_01