HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 3-bromo-4-(iodomethyl)-1-tert-pentyl-1H-pyrazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 3-bromo-4-(chloromethyl)-1-tert-pentyl-1H-pyrazole | HCID 67491560 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3-bromo-4-(iodomethyl)-1-tert-pentyl-1H-pyrazole | HCID 67491491 | 85% |
Reaction Steps
To a solution of 3-bromo-4-(chloromethyl)-1-tert-pentyl-1H-pyrazole (725 mg, 2.73 mmol) in acetone (25 mL) was added sodium iodide (4.09 g, 27.3 mmol). The reaction was heated at reflux for 2 hours, then cooled to room temperature and stirred overnight. The solvent was removed in vacuo and the residue was partitioned between ethyl acetate and water. The organic layer was washed with saturated aqueous sodium thiosulfate and brine. The organics were dried over sodium sulfate, filtered, and concentrated to yield the title compound (824 mg, 85%) as a brown oil. 1H NMR (400 MHz, CDCl3, δ): 7.47 (s, 1H), 4.26 (s, 2H), 1.83 (q, J=7.41 Hz, 2H), 1.50 (s, 6H), 0.67 (t, J=7.51 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09181252B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-0ad89ed1e50a473892794ab08f92f321 |
| Source note | uspto-grants-2015_11 |