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851069-96-0

(6-[4-(TRIFLUOROMETHOXY)PHENYL]PYRIDIN-3-YL)METHANOL synthesis

3synthesis methods
851069-97-1 Synthesis
6-[4-(TrifluoroMethoxy)phenyl]-3-pyridinecarbaldehyde

851069-97-1
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(6-[4-(TRIFLUOROMETHOXY)PHENYL]PYRIDIN-3-YL)METHANOL

851069-96-0
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Yield:851069-96-0 100%

Reaction Conditions:

with sodium tetrahydroborate in ethanol at 0 - 20; for 0.166667 h;

Steps:

9.a

6-(4-Trifluoromethoxy-phenyl)-pyridine-3-carbaldehyde (2.0 g, 7.48 mmol) was dissolved in EtOH (37 ml) and treated at 0° C. with NaBH4 (0.28 g, 7.48 mmol). After 10 min the cooling bath was removed and stirring was continued at ambient temperature. Pouring onto crashed ice, twofold extraction with AcOEt, washing with water, drying over sodium sulfate, and evaporation of the solvents afforded 2.08 g (7.7 mmol, quant.) of the title compound as off-white solid of mp. 57-58° C. MS: 269.1 (M)+.

References:

US2005/96353,2005,A1 Location in patent:Page/Page column 26

149806-06-4 Synthesis
2-Bromopyridine-5-carbaldehyde

149806-06-4
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(6-[4-(TRIFLUOROMETHOXY)PHENYL]PYRIDIN-3-YL)METHANOL

851069-96-0
23 suppliers
inquiry