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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 742615Generated: October 27, 2026

Acetonitrile → Bis(1,2,2,6,6-pentamethylpiperidin-4-yl) Azodicarboxylate

https://huagongshe.com/reaction/742615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantTrifluoroacetic acidHCID 6422—
ReactantIodo benzene diacetateHCID 12217721—
ReactantBis(1,2,2,6,6-pentamethylpiperidin-4-yl) Hydrazine-1,2-dicarboxylateHCID 53819262—
SolventDichloromethaneHCID 6344—
ProductBis(1,2,2,6,6-pentamethylpiperidin-4-yl) AzodicarboxylateHCID 5450859923.4%

Reaction Steps

To a solution of 30.0 g bis(1,2,2,6,6-pentamethylpiperidin-4-yl) hydrazine-1,2-dicarboxylate in 60 mL of methylene chloride is added 16.0 g (10.8 mL), of trifiuoroacetic acid at 0°-5° C., followed the addition of 22.6 g of iodobenzene diacetate at room temperature. After stirring at room temperature for 2.5 hours, the reaction mixture is washed with saturated sodium bicarbonate solution and then with brine, and dried over anhydrous magnesium sulfate. The dried solution is evaporated to afford a pale yellow oil. Trituration with acetonitrile affords 7.0 g of the title compound as a pale yellow solid; mp 135°-137° C. NMR and IR analyses are consistent with the desired structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05554754
Source datasetuspto-grants-1996_09
ORD IDord-96d0c6c4aaf8479fadff1c0bc672f05d
Source noteuspto-grants-1996_09