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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638258Generated: November 1, 2026

Pyridine → HCID 20068365, compound

https://huagongshe.com/reaction/1638258

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDichloromethaneHCID 6344—
ReactantHCID 20068382HCID 20068382—
Catalystchromium (VI) trioxideHCID 10219390—
SolventWaterHCID 962—
ProductHCID 20068365HCID 2006836512.3%

Reaction Steps

A solution of 42 parts of chromium(VI) oxide and 66 parts of pyridine in 665 parts of dichloromethane was stirred for 20 minutes at room temperature. A solution of 19 parts of α-ethyl-1-(1,2,3,4-tetrahydro-1-naphthalenyl)-1H-imidazole-5-methanol in 13.3 parts of dichloromethane was added dropwise to the thus obtained mixture. Upon complete addition, stirring was continued for 4 hours at room temperature. The reaction mixture was poured into water and the layers were separated. The organic layer was washed twice with water and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was dried for a long time in vacuo at 100° C., yielding 2.2 parts (12.3%) of 1-[1-(1,2,3,4-tetrahydro-1-naphthalenyl)-1H-imidazol-5-yl]-1-propanone as an oily residue (compound 2.53).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04878940
Source datasetuspto-grants-1989_11
ORD IDord-df318cb6573942c4acb90ed89a3771b9
Source noteuspto-grants-1989_11