Ammonium Chloride → (2-(Benzyloxy)-3-tert-butylphenyl)(3-(pyridin-2-yl)phenyl)methanol

A solution of 2-(3-bromophenyl)pyridine (2.4 g, 10.25 mmol) in anhydrous tetrahydrofuran (25 mL) was stirred at −78° C. and 2.5M n-butyllithium in hexanes (4.1 mL, 10.25 mmol) was added at such a rate that temperature did not exceed −70° C. Stirring was continued on the cold bath for 30 min and a solution of 2-(benzyloxy)-3-tert-butylbenzaldehyde (2.75 g, 10.25 mmol) in tetrahydrofuran (12 mL) was added at such a rate that temperature did not exceed −65° C. Stirring was continued on the cold bath for 20 min and 2 hr at room temperature. The reaction mixture was poured on saturated ammonium chloride (250 mL) and extracted with ethyl acetate (350 mL). The organic extract was washed with water (2×100 mL) and dried over sodium sulfate. The solvent was removed on a rotary evaporator and the crude product was used as such in the next step.

1. customdid not exceed −70° C
2. customdid not exceed −65° C
3. stirringStirring
4. waitwas continued on the cold bath for 20 min and 2 hr at room temperature
5. extractionextracted with ethyl acetate (350 mL)
6. extractionThe organic extract
7. washwas washed with water (2×100 mL)
8. dry with materialdried over sodium sulfate
9. customThe solvent was removed on a rotary evaporator

ORD-Eintrag

ord-5141c601919943c3abc47b2b3f3ac056

Quelldatensatz

uspto-grants-2013_09

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08541522B2