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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 866733Generated: October 25, 2026

Pyridine → 4-(4-t-Butylazo-4-cyanopentoxycarbonyl)phthalic Anhydride

https://huagongshe.com/reaction/866733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrimellitic anhydride chlorideHCID 70998—
Reactant4-t-Butylazo-4-cyanopentanolHCID 23345898—
SolventDiethyl EtherHCID 3283—
Product4-(4-t-Butylazo-4-cyanopentoxycarbonyl)phthalic AnhydrideHCID 54336890—

Reaction Steps

To a solution of 2.1 g. (0.01 m) of 4-chloroformylphthalic anhydride in 25 ml ether in a 50 ml 4-neck round bottom flask equipped with a condenser containing a CaCl2 drying tube, a thermometer, a magnetic stirring bar and a dropping funnel was added a solution of 2.0 g. (0.01 m) 2-t-butylazo-2-cyano-5-hydroxypentane (from XIV) and 0.8 g. (0.01 m) pyridine in 10 ml ether. This solution was added dropwise with stirring over 15 minutes holding the temperature between 15° and 22° C with a water bath. The reaction was stirred an additional hour after the addition was completed and the pyridine hydrochloride filtered off. The ether filtrate was dried over anhydrous Na2SO4, filtered and evaporated to dryness leaving 3.1 g. (84%) of a viscous liquid. The infrared spectrum contained 3 carbonyl bands and no OH bands.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04101522
Source datasetuspto-grants-1978_07
ORD IDord-0f9f4886c6584476adc3a7e77079ba51
Source noteuspto-grants-1978_07