HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705876Generated: October 30, 2026
Hydrogen Peroxide → 2-(4-(4-Chloro-3-(trifluoromethyl)phenoxy)phenyl)ethanol
https://huagongshe.com/reaction/705876
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | 9-Borabicyclo(3.3.1)nonane | HCID 78966 | — |
| Reactant | 1-Chloro-2-(trifluoromethyl)-4-(4-vinylphenoxy)benzene | HCID 66825837 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(4-(4-Chloro-3-(trifluoromethyl)phenoxy)phenyl)ethanol | HCID 66825529 | 69.2% |
Reaction Steps
To a solution of 1-chloro-2-(trifluoromethyl)-4-(4-vinylphenoxyl)benzene (3 g, 10.04 mmol) in THF (50 mL) was added 9-BBN (24.11 mL, 12.05 mmol) under nitrogen. The reaction mixture was stirred at 0° C. for 0.5 h, then the temperature was allowed to warm up to room temperature. NaOH (13.39 mL, 40.2 mmol) and H2O2 (14.36 mL, 141 mmol) was added. The mixture was then heated at 60° C. for 2 h. Na2SO3 was added to quench the reaction after cooling. Purification via flash chromatography then afforded the title compound (2.2 g, 6.95 mmol, 69.2% yield). LCMS: rt=3.55 min, [M+H+-H2O]=299
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09174968B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-c97fc9d0aa4d4dde97e816bffd6dcc61 |
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| Source note | uspto-grants-2015_11 |
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