反应详情

温度

60 °C

A solution of 1 g (3.86 mmol) of 2-(4-amino-phenyl)-1,1,1,3,3,3-hexafluoro-propan-2-ol in 2 ml of THF and 5 mL of pyridine was treated with 0.44 mL (4.63 mmol) of Ac2O and stirred for 2 hrs at 60° C. The solvent was evaporated and the crude distributed between a diluted aqueous solution of HCl and Et2O. the combined organic phases were dried over Na2SO4 and the solvent evaporated. The residue was dissolved in 5 mL of THF, treated with 7.7 mL of a 1M BH3*THF-solution in THF and refluxed for 2 hrs. The solvent was evaporated and the residue distributed between a diluted aqueous solution of NaOH and Et2O. The aqueous phase was then acidified by addition of an aqueous solution of HCl to a pH of ca. 7 and extracted with Et2O. The combined organic phases were dried over Na2SO4 and the solvent evaporated to give 1.07 g (96%) of crude 2-(4-ethylamino-phenyl)-1,1,1,3,3,3-hexafluoro-propan-2-ol, light yellow solid, MS: 288 (MH+).

1. customThe solvent was evaporated
2. dry with materialthe combined organic phases were dried over Na2SO4
3. customthe solvent evaporated
4. dissolutionThe residue was dissolved in 5 mL of THF
5. additiontreated with 7.7 mL of a 1M BH3*THF-solution in THF
6. temperaturerefluxed for 2 hrs
7. customThe solvent was evaporated
8. additionThe aqueous phase was then acidified by addition of an aqueous solution of HCl to a pH of ca. 7
9. extractionextracted with Et2O
10. dry with materialThe combined organic phases were dried over Na2SO4
11. customthe solvent evaporated