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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651735Generated: November 1, 2026

tert-Butylacrylamide → N-tert-butyl-[3-(N,N-dibenzylaminoxy)-propionamide]

https://huagongshe.com/reaction/1651735

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButylacrylamideHCID 7877—
ReactantDibenzylhydroxylamineHCID 69297—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductN-tert-butyl-[3-(N,N-dibenzylaminoxy)-propionamide]HCID 14297377—

Reaction Steps

A solution of 21.33 g of dibenzylhydroxylamine in 100 ml of dry tetrahydrofuran is admixed with 1.12 g of potassium-tert-butoxide followed by 12.70 g of N-tert-butylacrylamide. The solution is heated under reflux for 24 hours under N2. The crude reaction mixture is concentrated under reduced pressure and the residue is partitioned between water and methylene chloride. The organic layer is washed with water, brine dried (MgSO4) and evaporated under reduced pressure. Purification by liquid chromatography affords the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04929657
Source datasetuspto-grants-1990_05
ORD IDord-a3b3213a238e4063ba05771c94804dd4
Source noteuspto-grants-1990_05