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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602187Generated: October 29, 2026

3-[4-(4-Fluorophenoxy)benzyloxy]piperidine → Methyl 3-[3-[[4-(4-fluorophenoxy)phenyl]methoxy]piperidin-1-yl]benzoate

https://huagongshe.com/reaction/602187

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[4-(4-Fluorophenoxy)benzyloxy]piperidineHCID 58992695—
Reactant3-Methoxycarbonylphenylboric acidHCID 67170287—
ProductMethyl 3-[3-[[4-(4-fluorophenoxy)phenyl]methoxy]piperidin-1-yl]benzoateHCID 5899265942%

Reaction Steps

Using 3-[4-(4-fluorophenoxy)benzyloxy]piperidine (157 mg, 0.521 mmol) and 3-(methoxycarbonyl)phenylboric acid (187 mg, 1.04 mmol), the same procedure was followed as in Example 2 to give 94.8 mg (42%) of the desired compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902367B2
Source datasetuspto-grants-2011_03
ORD IDord-9fe8483d268b432081d988be7eb5d376
Source noteuspto-grants-2011_03