HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Diiodopropane → HCID 21316364, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Diiodopropane | HCID 12314 | — |
| Reactant | N,N,N-Trimethyl-3-(methylamino)propan-1-aminium bromide | HCID 21444211 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 21316364 | HCID 21316364 | — |
Reaction Steps
To a stirred solution of 216.2 mg. (1 mmole) of N,N,N-trimethyl-[3-(methylamino)]-1-propanaminium bromide in 1.5 ml. of acetonitrile is added a solution of 296 mg. (1 mmole) of 1,3-diiodopropane in 0.5 ml. of acetonitrile. The mixture is stirred at room temperature for 2.0 hours and the insoluble N,N,N-trimethyl-[3-(methylamino)]-1-propanaminium bromide hydrobromide is removed by filtration. The filtrate is evaporated and the solid residue obtained is extracted with methylene chloride. The methylene chloride extract is evaporated to give the oily product which is recrystallized from isopropanol-ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04156693 |
| Source dataset | uspto-grants-1979_05 |
| ORD ID | ord-9aa321de1a8344709dc6daf55ed49a04 |
| Source note | uspto-grants-1979_05 |