Water → 3-Bromo-4-(trifluoromethoxy)benzoic acid

HRID 2274043Notes

Reaction equation

HRID 2274043 reaction equation
[F:1][C:2]([F:14])([F:13])[O:3][C:4]1[CH:12]=[CH:11][C:7]([C:8]([OH:10])=[O:9])=[CH:6][CH:5]=1.[Br:15]Br.O>[N+](C)([O-])=O.[Fe](Cl)(Cl)Cl>[Br:15][C:5]1[CH:6]=[C:7]([CH:11]=[CH:12][C:4]=1[O:3][C:2]([F:13])([F:14])[F:1])[C:8]([OH:10])=[O:9]

Participants

6

Conditions

Temperature
110 °C

Procedure

4-(Trifluoromethoxy)benzoic acid (2 g, 9.70 mmol) and iron(III) chloride (1.574 g, 9.70 mmol) were suspended in nitromethane (20 mL). To this mixture was added bromine (0.497 mL, 9.70 mmol) at 0° C. The solution was heated under microwave irradiation at 110° C. for 2 h. The reaction mixture was added to cold water (100 mL) and extracted with ethylacetate (2×100 mL). The organic phase was washed with an aqueous solution of sodium thiosulfate pentahydrate and brine. The organic layer was concentrated and the residue was purified by HPLC to give the title compound as a white solid (1.5 g). LCMS m/z=287.0 [M+H]+; 1H NMR (400 MHz, DMSO-d6) δ ppm 7.67 (d, 1H), 8.06 (d, 1H), 8.29 (s, 1H), 13.47 (s, 1H).

Workup

  1. extractionextracted with ethylacetate (2×100 mL)
  2. washThe organic phase was washed with an aqueous solution of sodium thiosulfate pentahydrate and brine
  3. concentrationThe organic layer was concentrated
  4. customthe residue was purified by HPLC

Sources & evidence

ORD record
ord-56147d9de50c48b9acc6124577c9a370
Source dataset
uspto-grants-2015_09
Patent number
US09126932B2

Reaction notes

Loading…