HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethylamine → HCID 20272236, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | (3-Bromopropyl)triphenylphosphonium bromide | HCID 2723862 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20272236 | HCID 20272236 | — |
Reaction Steps
Into a one-liter 3-necked flask equipped with stirrer, condenser, addition funnel, and thermometer here was charged, 200 g of the above (3-bromopropyl)triphenylphosphonium bromide, and 650 ml ethanol. There was then added dropwise, 240 ml of diethylamine at 50° C. with stirring. After 18 hours at 65° C., the solution was concentrated to an oil and the residue was redissolved in 500 ml ethanol. The solution was again concentrated to a solid. The resulting brown solid was slurried in 500 ml of hot tetrahydrofuran and filtered. The crystal were recrystallized from tetrahydrofuran containing a small amount of ethanol to give 230 g of (3-diethylaminopropyl)triphenylphosphonium bromide hydrobromide (M.P. 239°-241° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04533722 |
| Source dataset | uspto-grants-1985_08 |
| ORD ID | ord-e9c4fead69c34d83820e56bb9cb70a11 |
| Source note | uspto-grants-1985_08 |