Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568564Generated: October 25, 2026

Ammonium Chloride → 1-(p-N-tert-butylaminocarbonylphenyl)-4-(1-trityl-4-imidazolyl)-1-butanone

https://huagongshe.com/reaction/568564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant4-bromo-N-tert-butylbenzamideHCID 603258—
Reactant4-(1-Trityl-1H-imidazol-4-YL)-butyric acidHCID 11395367—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1-(p-N-tert-butylaminocarbonylphenyl)-4-(1-trityl-4-imidazolyl)-1-butanoneHCID 54304392—

Reaction Steps

6,95 g of N-tert-butyl-p-bromobenzamide is dissolved in 175 ml of tetrahydrofuran at -70° under nitrogen and 20.1 ml of n-butyllithium (2.7M) is added dropwise. After 30 min, a solution of 5.35 g of 4-(1-trityl-4-imidazolyl)-butanoic acid in 10 ml of tetrahydrofuran is added slowly. The reaction mixture is allowed to warm slowly to room temperature and 20 ml of an aqueous ammonium chloride solution is added. The organic layer is separated, dried over sodium sulfate and evaporated to yield 1-(p-N-tert-butylaminocarbonylphenyl)-4-(1-trityl-4-imidazolyl)-1-butanone

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04728645
Source datasetuspto-grants-1988_03
ORD IDord-aff92d63a08445a1a2f661a94f2883ea
Source noteuspto-grants-1988_03