HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 2,6-Bis(trifluoromethyl)benzyl bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2,6-Bis(trifluoromethyl)benzenemethanol | HCID 15346431 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,6-Bis(trifluoromethyl)benzyl bromide | HCID 11851363 | — |
Reaction Steps
To 1 ml of a mixture of 48% aqueous HBr solution and conc. sulfuric acid (2:1 v/v) were added 0.81 g (3.3 mmol) (2,6-bis-trifluoromethyl-phenyl)-methanol and the solution heated to reflux for 6 h. Then the reaction mixture was cooled to rt, diluted with water and extracted with tert-butyl methyl ether. The combined extracts were washed with brine, dried over Na2SO4, filtered and evaporated. Kugelrohr distillation provided 2-bromomethyl-1,3-bis-trifluoromethyl-benzene as colourless oil of b.p. 135-140° C./22 mbar: MS (EI): 307.9 and 305.9 (M+.), 227.1 (((M-Br)+.), 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07875645B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-857bd6fca37f40abb00df775daeefabd |
| Source note | uspto-grants-2011_01 |