HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 1-Benzyl-1H-pyrazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Iodopyrazole | HCID 77022 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Benzyl-1H-pyrazole | HCID 3546441 | — |
Reaction Steps
To a solution of 4-iodopyrazole (400 mg, 2 mmol) in DMF(4 mL) at 0 C. was added sodiumhydride (80 mg, 60% dispersion in mineral oil, 2 mmol) followed by benzyl bromide (342 mg, 2 mmol) and reaction micture was allowed to stir for 2 h. Reaction mixture was concentrated in vacuo and the residue was purified by column chromatography to give N-benzylpyrazole in almost quantitative yield. IH NMR 5.29 (s, 2H), 7.18-7.28 (m,2H), 7.28-7.40 (m, 4H), 7.53 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06214807B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-8d57ba5625224e77bbf09491aeee0cc6 |
| Source note | uspto-grants-2001_04 |