1-BROMO-4-(2,2,2-TRIFLUOROETHOXY)BENZENE
1-BROMO-4-(2,2,2-TRIFLUOROETHOXY)BENZENE Basic information
- Product Name:
- 1-BROMO-4-(2,2,2-TRIFLUOROETHOXY)BENZENE
- Synonyms:
-
- 1-BROMO-4-(2,2,2-TRIFLUOROETHOXY)BENZENE
- UKRORGSYN-BB BBV-081072
- 4-(2,2,2-Trifluoroethoxy)bromobenzene
- Benzene, 1-bromo-4-(2,2,2-trifluoroethoxy)-
- 4-bromo-1-(2,2,2-trifluoroethoxy)benzene
- 4-(Trifluoroethoxy)bromobenzene
- CAS:
- 106854-77-7
- MF:
- C8H6BrF3O
- MW:
- 255.03
- Mol File:
- 106854-77-7.mol
1-BROMO-4-(2,2,2-TRIFLUOROETHOXY)BENZENE Chemical Properties
- Boiling point:
- 212.8±40.0 °C(Predicted)
- Density
- 1.569±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- Appearance
- White to off-white Solid
- InChI
- InChI=1S/C8H6BrF3O/c9-6-1-3-7(4-2-6)13-5-8(10,11)12/h1-4H,5H2
- InChIKey
- SMDIDUHBHCDCRQ-UHFFFAOYSA-N
- SMILES
- C1(Br)=CC=C(OCC(F)(F)F)C=C1
1-BROMO-4-(2,2,2-TRIFLUOROETHOXY)BENZENE Usage And Synthesis
Synthesis
106-41-2
6226-25-1
106854-77-7
General procedure for the synthesis of 1-bromo-4-(2,2,2-trifluoroethoxy)benzene from 4-bromophenol and 2,2,2-trifluoroethyl trifluoromethanesulfonate: first, 4-bromophenol (9.57 g, 55 mmol) was dissolved in acetone (200 mL), followed by the addition of potassium carbonate (22.89 g, 166 mmol) and 2,2,2-trifluoroethyl trifluoromethanesulfonate ester (16.0 g, 69 mmol). The reaction mixture was stirred at room temperature overnight. Upon completion of the reaction, the mixture was filtered to remove the insoluble salt and then concentrated under reduced pressure at 300 mbar at 30 °C to remove the acetone. The final product was 1-bromo-4-(2,2,2-trifluoroethoxy)benzene as a waxy solid (more than 100% yield, as a small amount of acetone remained in the product).
References
[1] Patent: WO2005/822, 2005, A1. Location in patent: Page/Page column 44
[2] Patent: US2016/332999, 2016, A1. Location in patent: Paragraph 0576; 0577
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