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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252251Generated: November 1, 2026

Benzyl Bromide → 4-amino-N-benzyl-N-methyl-2-oxo-3-pentenesulfonamide

https://huagongshe.com/reaction/1252251

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant4-amino-N-methyl-2-oxo-3-pentenesulfonamideHCID 73663808—
SolventDimethylformamideHCID 6228—
Product4-amino-N-benzyl-N-methyl-2-oxo-3-pentenesulfonamideHCID 70045034—

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 3.6 ml of benzyl bromide in 50 ml of dimethylformamide was treated with 6 g of potassium carbonate and the mixture was stirred intensively at room temperature for 9 hours. The product was firstly chromatographed on 300 g of silica gel with ethyl acetate as the elution agent and then recrystallized from isopropanol. There were obtained 3.4 g of 4-amino-N-benzyl-N-methyl-2-oxo-3-pentenesulfonamide in the form of colorless crystals, m.p. 115°-118°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04742069
Source datasetuspto-grants-1988_05
ORD IDord-8cb9429ee40943b9b609b38b501c7db4
Source noteuspto-grants-1988_05