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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2256311Generated: November 1, 2026

1,1'-Carbonyldiimidazole → 1-[3-(3,4-Dichlorophenyl)-5-hydroxy-1-oxopentyl]-1,2,3,4-tetrahydroquinoline

https://huagongshe.com/reaction/2256311

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 19029335HCID 19029335—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product1-[3-(3,4-Dichlorophenyl)-5-hydroxy-1-oxopentyl]-1,2,3,4-tetrahydroquinolineHCID 19029371166.8%

Reaction Steps

Beta-(3,4-Dichlorophenyl)-1,2,3,4-tetrahydro-delta-oxo-quinolinepentanoic acid (14.3 g) in EtOAc (300 mL) was treated with carbonyldiimidazole (7.42 g) and N,N-dimethylaminopyridine (450 mg). The resulting solution was stirred at room temperature for 15 minutes and then heated at 50° C. for two hours. The reaction mixture was cooled to 0° C. and treated with a solution of NaBH4 (5.5 g) in H2O (100 mL), warmed slowly to room temperature and stirred for 12 hours. The reaction mixture was diluted with EtOAc (500 mL) and washed with 1N HCl (1×200 mL), sat. NaHCO3 (1×200 mL) and water (1×200 mL). The organic phase was dried over MgSO4, filtered and concentrated under reduced pressure to yield the crude compound as a oil. Silica gel chromatography eluting with 0-10% MeOH/CH2Cl2 gave the title compound (11.5 g). Mass spectrum (CI): 378.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05654316
Source datasetuspto-grants-1997_08
ORD IDord-1e1954af544e43818f2e7ecd13428893
Source noteuspto-grants-1997_08