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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252252Generated: November 1, 2026

Allyl bromide → N-allyl-N-methyl-4-amino-2-oxo-3-pentenesulfonamide

https://huagongshe.com/reaction/1252252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactant4-amino-N-methyl-2-oxo-3-pentenesulfonamideHCID 73663808—
SolventDimethylformamideHCID 6228—
ProductN-allyl-N-methyl-4-amino-2-oxo-3-pentenesulfonamideHCID 73663809—

Reaction Steps

In accordance with the procedure described in Example 7, a solution of 3.8 g of 4-amino-N-methyl-2-oxo-3-pentenesulfonamide and 2.5 ml of allyl bromide in 50 ml of dimethylformamide was treated with 6 g of potassium carbonate and the mixture was stirred intensively at room temperature for 7 hours. The product was firstly chromatographed on 300 g of silica gel with methylene chloride/ethyl acetate (4:1) as the elution agent and then recrystallized from methylene chloride/ether. There were obtained 3.3 g of N-allyl-N-methyl-4-amino-2-oxo-3-pentenesulfonamide in the form of colorless crystals, m.p. 86°-89°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04742069
Source datasetuspto-grants-1988_05
ORD IDord-2600abd8c1624937bae69247c52d2514
Source noteuspto-grants-1988_05