HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron tribromide → 3-methyl-4-(4-(trifluoromethyl)-1H-pyrazol-1-yl)phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 1-(4-methoxy-2-methylphenyl)-4-(trifluoromethyl)-1H-pyrazole | HCID 68156642 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-methyl-4-(4-(trifluoromethyl)-1H-pyrazol-1-yl)phenol | HCID 65313798 | 99% |
Reaction Steps
To a 0° C. solution of 1-(4-methoxy-2-methylphenyl)-4-(trifluoromethyl)-1H-pyrazole (400 mg, 2 mmol) in dichloromethane (5 mL) was added boron tribromide (1 g, 6 mmol). The mixture was allowed to warm to room temperature and stir overnight. The reaction was quenched with methanol (2 mL), diluted with water (10 mL), and extracted with dichloromethane (3×10 mL). The combined organics were dried over sodium sulfate, filtered, and concentrated to give 3-methyl-4-(4-(trifluoromethyl)-1H-pyrazol-1-yl)phenol (390 mg, 99%) as a brown solid. 1H NMR (400 MHz, CDCl3, δ): 7.83 (s, 1H), 7.74 (s, 1H), 7.08 (d, J=8.4 Hz, 1H), 6.65 (s, 1H), 6.62 (d, J=8.4 Hz, 1H), 5.57 (s, 1H), 2.05 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08859591B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-368c813a2e3546e2836653544f263d48 |
| Source note | uspto-grants-2014_10 |