Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2062637Generated: November 2, 2026

Chlorobenzene → HCID 178438666, compound

https://huagongshe.com/reaction/2062637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorobenzeneHCID 7964—
ReactantN,N,N-Tributylbutan-1-aminium fluoride--hydrogen fluoride (1/1/2)HCID 11748636—
ReactantPotassium fluoride, 99%, spray-driedHCID 53443437—
ReactantHCID 178438598HCID 178438598—
SolventTolueneHCID 1140—
ProductHCID 178438666HCID 17843866660%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 4′-({4-[trans-4-(oxiran-2-ylmethoxy)cyclohexyl]-5-oxo-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl}methyl)biphenyl-2-carbonitrile (0.25 g), potassium hydrogen fluoride (0.075 g), tetra-n-butylammonium dihydrogentrifluoride (0.015 g) and chlorobenzene (1 mL) was stirred at 120° C. for 5 hr. Potassium hydrogen fluoride (0.075 g) and tetra-n-butylammonium dihydrogentrifluoride (0.014 g) were added, and the mixture was stirred at 120° C. for 16 hr. Toluene was added, and the precipitate was filtered off. The filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography to give the title compound as a colorless solid (0.15 g, 60%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08283353B2
Source datasetuspto-grants-2012_10
ORD IDord-be0fe05418cc40be81371e2521c6f1b3
Source noteuspto-grants-2012_10