Diisobutylaluminum hydride → (E)-3-(3,5-difluoro-4-phenoxyphenyl)-2-methylprop-2-en-1-ol

To a solution of (E)-ethyl 3-(3,5-difluoro-4-phenoxyphenyl)-2-methylacrylate (Intermediate 41.2) (800 mg, 2.51 mmol) in dry DCM (25 mL) under N2 at −78° C. was added a solution of DIBAL-H (8.79 mL, 1M in DCM) dropwise over several minutes. The reaction was allowed to warm to room temperature over 2 hours. The reaction mixture was cooled to 0° C., quenched with 25 mL of Rochelle's Salt solution (10% w/v in water), and stirred vigorously for 1 hour. The resulting suspension was diluted with water (20 mL) and extracted with DCM (3×30 mL). The combined organic layers were dried over Na2SO4 and concentrated. The resulting oil was applied onto a silica gel column (50% EtOAc in hexanes) to yield 566 mg of the title compound (82%) as a yellow oil.

1. temperatureThe reaction mixture was cooled to 0° C.
2. customquenched with 25 mL of Rochelle's Salt solution (10% w/v in water)
3. additionThe resulting suspension was diluted with water (20 mL)
4. extractionextracted with DCM (3×30 mL)
5. dry with materialThe combined organic layers were dried over Na2SO4
6. concentrationconcentrated

ORD record

ord-fed5d5b52691416db64b00fc31a05345

Source dataset

uspto-grants-2013_09

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08541448B2