HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 20240740, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | HCID 20240737 | HCID 20240737 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 20240740 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04554006 |
| Source dataset | uspto-grants-1985_11 |
| ORD ID | ord-8c34436e06e2463f839ab12401028216 |
| Source note | uspto-grants-1985_11 |