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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2,2'-Dihydroxybenzophenone | HCID 70038 | — |
| Reactant | 4-[(E)-tert-Butyldiazenyl]-4-cyanopentanoyl chloride | HCID 15274024 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Pentane | HCID 8003 | — |
| Product | 2-(4-t-Butylazo-4-cyanovaleryloxy)-2'-hydroxybenzophenone | HCID 22756219 | 71.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04045426 |
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| Source dataset | uspto-grants-1977_08 |
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| ORD ID | ord-cbe8ee5b14404ad487ded47d33b5e99b |
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| Source note | uspto-grants-1977_08 |
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