HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 86638088, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | HCID 16248957 | HCID 16248957 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 86638088 | HCID 86638088 | 200.7% |
Reaction Conditions
| Temperature | 140 °C |
|---|
Reaction Steps
A microwave vial was charged with 2-chloromethyl-5,7-dimethyl-imidazo[1,2-a]pyrimidine hydrochloride (500 mg, 2.15 mmol), and 1,2-dichloroethane (16 mL) and argon was bubbled through the mixture. To this mixture was added 1,8-diazabicyclo[5.4.0]undec-7-ene (0.350 mL, 2.34 mmol) and triphenylphosphine (848 mg, 3.23 mmol). The vial was sealed with a crimp-on cap and the mixture was heated at 140° C. for 1 hour using a microwave synthesizer. Evaporation of volatiles afforded crude (5,7-dimethyl-imidazo[1,2-a]pyrimidin-2-ylmethyl)-triphenyl-phosphonium chloride as a dark grey solid (1.976 g) which was used without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09018217B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-7cafd7b07bee42b1a177906b40616d7b |
| Source note | uspto-grants-2015_04 |