HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenethyl bromide → HCID 10315211, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 10421619 | HCID 10421619 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 10315211 | HCID 10315211 | — |
Reaction Steps
To a solution of 11-amino-4,5-dihydro-1H-pyrazolo[3,4-a]acridine (4.36 g) in dry DMF (130 ml) was slowly added 922 mg of NaH (60%). The reaction was stirred at room temperature for one hour, then (2-bromoethyl)benzene (3.23 ml) was added and the reaction stirred for four hours. An additional 230 mg of NaH (60%) was added, and then the reaction was stirred for a half hour, after which 0.8 ml of (2-bromoethyl)benzene was added and the reaction was stirred at room temperature overnight.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05179100 |
| Source dataset | uspto-grants-1993_01 |
| ORD ID | ord-5de56d08bc0440ddbde840e2cb76db6a |
| Source note | uspto-grants-1993_01 |