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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210705Generated: October 30, 2026

tert-Butyl 3-oxo-2-phenylpiperidine-1-carboxylate → HCID 19379354, compound

https://huagongshe.com/reaction/2210705

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 3-oxo-2-phenylpiperidine-1-carboxylateHCID 11414684—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19379354HCID 19379354—

Reaction Steps

A solution of 1-t-butoxycarbonyl-2-phenyl-piperidin-3-one (0.57 g, Example 48a)in 5 ml anhydrous tetrahydrofuran at -78° C. was treated with methyl magnesium bromide (1.6 ml of 1.5M solution in toluene-THF). The reaction was partitioned between saturated ammonium chloride-diethyl ether, the organic phase dried and evaporated in vacuo. The residue was chromatographed using 20% ethyl acetate in hexane as eluant to give 1-t-butoxycarbonyl, 3-methyl-2-phenyl piperidin-3-ol as a crystalline solid, m.p.=95°-97° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05459270
Source datasetuspto-grants-1995_10
ORD IDord-ef5917e872314a859669994d23f119e2
Source noteuspto-grants-1995_10