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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260552Generated: October 30, 2026

Trityl chloride → HCID 22915640, compound

https://huagongshe.com/reaction/2260552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
ReactantSodium HydroxideHCID 14798—
ReactantTributyltin ChlorideHCID 15096—
ReactantSodium AzideHCID 33557—
Reactant2-(6-Methylquinolin-2-yl)benzonitrileHCID 21804239—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
ProductHCID 22915640HCID 22915640377.6%

Reaction Steps

3.5 ml of toluene were added to 855 mg (3.5 mmol) of 2-(6-methyl-quinolin-2-yl)benzonitrile obtained in Reference Example 8. To the mixture were further added 0.24 g (0.68 mmol) of sodium azide and 1 ml (3.83 mmol) of tributyltin chloride. After heating under reflux for 45 hours, the mixture was allowed to cool and diluted with 7 ml of toluene. To the mixture were added 0.4 ml (4 mmol) of a 10N sodium hydroxide aqueous solution and 1.01 g (3.61 mmol) of tritylchloride with stirring. After stirring at room temperature for 1.5 hours, 15 ml of hexane were added to the mixture and the solid material was collected by filtration. The thus obtained solid material was washed with 10 ml of water twice and then 5 ml of methanol three times. The filter cake was dried under vacuum to obtain 1.36 g of 5-[2-(6-methylquinolin-2-yl)phenyl] -2-triphenylmethyl-2H-tetrazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05478832
Source datasetuspto-grants-1995_12
ORD IDord-590f50a7dc1b4dcd936a11fc03322612
Source noteuspto-grants-1995_12