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81151-35-1

4-[(4-FLUOROBENZYL)OXY]PIPERIDINE synthesis

3synthesis methods
tert-butyl 4-((4-fluorobenzyl)oxy)piperidine-1-carboxylate

1121587-29-8
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4-[(4-FLUOROBENZYL)OXY]PIPERIDINE

81151-35-1
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Yield:81151-35-1 0.5 g

Reaction Conditions:

with hydrogenchloride in tetrahydrofuran;lithium hydroxide monohydrate at 20; for 1 h;

Steps:

247.B

B. To a solution of tert-butyl 4-((4-fluorobenzyl)oxy)piperidine-1-carboxylate (800 mg, 2.59 mmol) in THF (2 mL) was added con hydrogen chloride (2 mL). The reaction was stirred at ambient temperature for 1 h. Saturated aqueous NaHCO3 (30 mL) and DCM (200 mL) were added to the reaction vessel and the resulting biphasic mixture was transferred to a separatory funnel. The layers were separated and the organic phase was washed with saturated aqueous NaCl (2 x 20 mL). The combined organics were dried over anhydrous Na2SO4, filtered and concentrated in vacuo to provide 4-((4-fluorobenzyl)oxy)piperidine (0.5 g, 2.39 mmol) as a green oil.

References:

WO2018/26371,2018,A1 Location in patent:Paragraph 0311

109384-19-2 Synthesis
N-BOC-4-Hydroxypiperidine

109384-19-2
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4-[(4-FLUOROBENZYL)OXY]PIPERIDINE

81151-35-1
8 suppliers
inquiry