HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075014Generated: October 30, 2026
Carbon tetrabromide → 1-Bromo-2-(bromomethyl)-4-(trifluoromethyl)benzene
https://huagongshe.com/reaction/2075014
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Bromo-5-(trifluoromethyl)benzyl alcohol | HCID 2756248 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Bromo-2-(bromomethyl)-4-(trifluoromethyl)benzene | HCID 2756249 | 70.1% |
Reaction Steps
To a solution of (2-bromo-5-(trifluoromethyl)phenyl)methanol (4.7 g, 18 mmol) in methylene chloride (50 mL) at −10° C. was added carbon tetrabromide (CBr4) (7.17 g, 21.6 mmol). The resulting mixture was stirred at −10° C. for 15 minutes. Triphenylphosphine (5.61 g, 21.4 mmol) was then slowly added portionwise. This mixture was stirred at room temperature for 16 hours. The mixture was partitioned between saturated ammonium chloride (NH4Cl) (50 ml) and methylene chloride (2×50 mL). The combined organic layers were washed with saturated NaCl (50 mL), dried (MgSO4) and concentrated. The residue was purified by flash chromatography (silica gel) (eluted with 3:1 hexanes-ethyl acetate) to yield the title compound as a white solid (4.01 g). 1H NMR (400 MHz, CDCl3) δ 4.6 (s, 2H) 7.5 (dd, J=8.3, 1.6 Hz, 1H) 7.8 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07919506B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-301daa5019ac463bb51218ea12bbb7ec |
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| Source note | uspto-grants-2011_04 |
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