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ChemicalBook CAS DataBase List (4-Bromo-2-(trifluoromethoxy)phenyl)methanol
220996-81-6

(4-Bromo-2-(trifluoromethoxy)phenyl)methanol synthesis

1synthesis methods
4-Bromo-2-(trifluoromethoxy)benzaldehyde

220996-80-5

(4-Bromo-2-(trifluoromethoxy)phenyl)methanol

220996-81-6

[Step 2] Synthesis of (4-bromo-2-(trifluoromethoxy)phenyl)methanol: To a solution of 4-bromo-2-(trifluoromethoxy)benzaldehyde (16 g, 59 mmol) in methanol (0.23 L) was added sodium borohydride (2.4 g, 63 mmol) in batches at -10 °C. The reaction solution was stirred at -10 °C for 10 min before acetone (10 mL) and 1N hydrochloric acid (10 mL) were added sequentially to quench the reaction. The reaction mixture was concentrated under reduced pressure and water was added to the residue and extracted with ethyl acetate. The organic layers were combined, dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography (elution gradient: hexane/ethyl acetate = 50:1 → 1:1) to afford 15 g (91% yield) of the title compound (4-bromo-2-(trifluoromethoxy)phenyl)methanol (hereinafter referred to as Reference Example Compound 2).

220996-80-5 Synthesis
4-Bromo-2-(trifluoromethoxy)benzaldehyde

220996-80-5
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-

Yield:220996-81-6 95%

Reaction Conditions:

with sodium tetrahydroborate in methanol;

References:

Williams, Peter D.;Bock, Mark G.;Evans, Ben E.;Freidinger, Roger M.;Gallicchio, Steven N.;Guidotti, Maribeth T.;Jacobson, Marlene A.;Michelle S, Kuo;Levy, Michelle R.;Edward V, Lis;Michelson, Stuart R.;Pawluczyk, Joseph M.;Perlow, Debra S.;Pettibone, Douglas J.;Quigley, Amy G.;Reiss, Duane R.;Salvatore, Christopher;Stauffer, Kenneth J.;Woyden, Carla J. [Bioorganic and Medicinal Chemistry Letters,1999,vol. 9,# 9,p. 1311 - 1316]