Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 67196817 | HCID 67196817 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67197113 | HCID 67197113 | — |
Reaction Steps
1-(4-Methoxyphenyl)-5-styryl-3-trifluoromethyl-1H-pyrazole (0.14 g, 0.4 mmol) was dissolved in dichloromethane (1.2 mL) and cooled to −40° C. Boron tribromide (1.2 mL, 1 M in dichloromethane, 1.2 mmol) was added, and the reaction was stirred overnight, warming up to room temperature. Saturated sodium bicarbonate solution was added, and the mixture was extracted with ethyl acetate. The extracts were dried over MgSO4 and concentrated. The reaction was assumed to be quantitative. LC-MS (C18H13F3N2O calculated 330) m/z 331 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07981896B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-9e60f4cac811467b861a7bc617532158 |
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| Source note | uspto-grants-2011_07 |
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