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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 967770Generated: October 31, 2026

1-Benzyl-4-(4-carboxyphenoxymethyl)piperidin-4-ol → 1-Benzyl-4-(4-methoxycarbonylphenoxymethyl)piperidin-4-ol

https://huagongshe.com/reaction/967770

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-(4-carboxyphenoxymethyl)piperidin-4-olHCID 22291294—
ReactantTrimethylsilyldiazomethane hexaneHCID 86587183—
SolventMethanolHCID 887—
Product1-Benzyl-4-(4-methoxycarbonylphenoxymethyl)piperidin-4-olHCID 22291265—

Reaction Steps

The compound (0.86 g) obtained in Step 4 was dissolved in methanol (10 mL) and to the solution was added a 2M trimethylsilyidiazomethan-hexane solution (1.3 mL). After completion of the reaction, the residue from which the solvent was removed under reduced pressure was purified by silica gel column chromatography (Chromatorex NH™) (eluent; ethyl acetate:hexane=1:19 to 1:9) to obtain the titled compound (0.8 g) as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06956046B2
Source datasetuspto-grants-2005_10
ORD IDord-977f295bf3f34f6e9fe71dfc1a2dc284
Source noteuspto-grants-2005_10