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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1412413Generated: October 29, 2026

Chlorobenzene → HCID 178438666, compound

https://huagongshe.com/reaction/1412413

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 numberUS08921379B2
Source datasetuspto-grants-2014_12
ORD IDord-2769301d1cd744629e9b2ee2da6669b8
Source noteuspto-grants-2014_12