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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537227Generated: October 30, 2026

tert-Butyl 4-oxopiperidine-1-carboxylate → tert-Butyl 4-hydroxy-4-(3-methoxyphenyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/537227

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantHCID 178490745HCID 178490745—
Producttert-Butyl 4-hydroxy-4-(3-methoxyphenyl)piperidine-1-carboxylateHCID 4976024255%

Reaction Steps

This compound was prepared from tert-Butyl 4-oxopiperidine-1-carboxylate and 3-methoxyphenylmagnesium bromide as described in Step 1 of Example 6 in 55% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859777B2
Source datasetuspto-grants-2014_10
ORD IDord-c21be25e33c04ffbad1b1426124cdd12
Source noteuspto-grants-2014_10