HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822328Generated: November 1, 2026
Boron tribromide → 2-Phenoxy-3-trifluoromethyl-phenol
https://huagongshe.com/reaction/1822328
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 2-Phenoxy-3-trifluoromethyl-anisole | HCID 69076100 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Phenoxy-3-trifluoromethyl-phenol | HCID 54172852 | 46% |
Reaction Steps
A −78° C. solution of the crude 2-phenoxy-3-trifluoromethyl-anisole (3.47 g, 12.9 mmol) in CH2Cl2 (35 mL) is treated with BBr3 (12.99 g, 51.8 mmol), and the mixture is warmed to 0° C. and stirred for 1.5 h under N2. The reaction is poured into ice water and then extracted with Et2O. The organic layer is dried (Na2SO4), and the solvent is removed in vacuo to afford crude material that is absorbed on silica gel and columned with 96/4 chloroform/methyl tert-butyl ether to afford 1.51 g (24%) of 2-phenoxy-3-trifluoromethyl-phenol. Rf=0.34 (96/4 chloroform/methyl tert-butyl ether). 1H NMR (400 MHz, CDCl3); MS (ES−+) m/z mass calculated for C13H9O2F3 254, found 253 (M+1, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07608639B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-924a77610ca34f3e91deb041e08a6521 |
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| Source note | uspto-grants-2009_10 |
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