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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583700Generated: November 1, 2026

Allyl bromide → HCID 20240740, compound

https://huagongshe.com/reaction/1583700

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantHCID 20240737HCID 20240737—
SolventEthyl AcetateHCID 8857—
ProductHCID 20240740HCID 20240740—

Reaction Steps

A solution of 51 g of N-[2-methyl-3-(o-methyl-phenyl)-propyl]-pyrrolidine and 58 g of allyl bromide in 200 ml of ethyl acetate is refluxed for 5 hours. The product precipitates as a resin. After the ethyl acetate has been decanted, the crude product is triturated several times with ethyl acetate. Supernatant solvent is decanted. Finally, the product is triturated with n-pentane and the solvent decanted. The oil which remains is freed from solvent residues in a rotary evaporator. There remains 60 g of N-allyl-N-[2-methyl-3-(o-methyl-phenyl)-propyl]-pyrrolidinium bromide as a brown resin.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04554006
Source datasetuspto-grants-1985_11
ORD IDord-8c34436e06e2463f839ab12401028216
Source noteuspto-grants-1985_11