Sodium Hydroxide → 2-(Trifluoromethoxy)phenylboronic Acid (contains varying amounts of Anhydride)

Temperature

-78 °C

To a stirred solution of 2 g (9.5 mmol) of 1-bromo-2-trifluoromethoxy benzene in 28 Ml of tetrahydrofuran (THF) at −78° C., was carefully added a solution of 5.9 Ml of a 1.7 M solution of t-butyl lithium in hexanes (9.5 mmol). This reaction mixture was stirred at −78° C. for 45 min. To this reaction mixture at −78° C. was added 2.58 Ml (11.1 mmol) of tri-isopropyl borate and the mixture was slowly warmed to room temperature (RT) over a period of 16 h. The reaction mixture was diluted with water and made basic with 2N NaOH solution. The reaction mixture was washed with EtOAc. The aqueous fraction was acidified with 2N HCl solution and stirred for 1 h at RT. The reaction mixture was extracted with EtOAc and the organic fractions were washed with water, saturated NaCl solution (brine), dried over Na2SO4 and filtered. The filtrate was concentrated to give the title compound as a white solid. 1HNMR (CDCl3) (δ, ppm): 7.96 (dd, J=7.2, 1.6 Hz, 1 H), 7.53 (ddd, J=9.1, 7.3, 1.8 Hz, 1 H), 7.38 (td, J=7.3, 0.7 Hz, 1 H), 7.28 (d, J=8.2 Hz, 1H), 5.25 (br s, 2 H). MS (M+H): 206.9.

1. temperaturethe mixture was slowly warmed to room temperature (RT) over a period of 16 h
2. washThe reaction mixture was washed with EtOAc
3. stirringstirred for 1 h at RT
4. extractionThe reaction mixture was extracted with EtOAc
5. washthe organic fractions were washed with water, saturated NaCl solution (brine)
6. dry with materialdried over Na2SO4
7. filtrationfiltered
8. concentrationThe filtrate was concentrated

ORD record

ord-f775b3b9f3c143e9bcc006e4aa5c9112

Source dataset

uspto-grants-2009_08

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07572822B2