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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442309Generated: October 26, 2026

Pyridine → 2-(4-t-Butylazo-4-cyanovaleryloxy)-2'-hydroxybenzophenone

https://huagongshe.com/reaction/442309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2,2'-DihydroxybenzophenoneHCID 70038—
Reactant4-[(E)-tert-Butyldiazenyl]-4-cyanopentanoyl chlorideHCID 15274024—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventPentaneHCID 8003—
Product2-(4-t-Butylazo-4-cyanovaleryloxy)-2'-hydroxybenzophenoneHCID 2275621971.2%

Reaction Steps

To a solution of 4.68 g. (0.0218 m) of 2,2'-dihydroxybenzophenone and 2.5 ml of pyridine in 30 ml of ether in a 4 neck 100 ml round bottom flask equipped with a thermometer, condenser and magnetic stirring bar was added 5.0 g. (0.0218 m) of 4-t-butylazo-4-cyanovaleryl chloride dropwise with cooling so the temperature did not rise above 25° C. After completion of the addition the reaction mixture was stirred 1/2 hour at room temperature and then diluted with 100 ml of water. The ether layer was separated, washed consecutively with 5% HCl, water, 10% NaHCO3 solution and saturated sodium chloride solution. The ether was evaporated off leaving a yellow solid. The solid was slurried in pentane, filtered and air dried. The product weighed 6.3 g. (71.2% yield) and decomposed slowly on heating above 80° C. The infrared spectrum of the product was in agreement with the structure of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04045426
Source datasetuspto-grants-1977_08
ORD IDord-cbe8ee5b14404ad487ded47d33b5e99b
Source noteuspto-grants-1977_08