HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 21466821, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-Oxazolemethanol, 4,5-dihydro-2,4-dimethyl- | HCID 98073 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21466821 | HCID 21466821 | — |
Reaction Steps
A solution of 40.1 g (310 mmol) of 2,4-dimethyl-4-hydroxymethyl-2-oxazoline (J. Nys and J. Libeer, Bull. Soco Chim. Belg., 65, 377 (1956)) and 85.5 g (326 mmol) of triphenylphosphine in 400 ml of dichloromethane is mixed at 0° C. in portions with 58.0 g (326 mmol) of N-bromosuccinimide and then stirred overnight at room temperature. The solution is concentrated by evaporation and the residue is pulverized with tert-butyl methyl ether. A precipitate develops, which is separated and washed with tert-butyl methyl ether. The combined filtrates are subjected to a fractionated distillation at normal pressure, and first the solvent is drawn off and then the title compound is distilled at an oil bath temperature of 200° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05695737 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-8bd1310b68e74a268dc196b72ce1e5ab |
| Source note | uspto-grants-1997_12 |