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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815844Generated: October 26, 2026

1-Benzyl-3-methyl-4-piperidone → 1-Benzyl-3-methyl-4-hydroxy-4-(5-chlorobenzofur-7-yl)piperidine

https://huagongshe.com/reaction/1815844

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-3-methyl-4-piperidoneHCID 560965—
Reactant7-Bromo-5-chloro-1-benzofuranHCID 22144720—
Product1-Benzyl-3-methyl-4-hydroxy-4-(5-chlorobenzofur-7-yl)piperidineHCID 2249563192%

Reaction Steps

Beginning with 4.0 gm (17.3 mMol) 5-chloro-7-bromobenzofuran and 3.86 gm (19.0 mMol) 1-benzyl-3-methyl-4-oxo-piperidine, 5.6 gm (92%) of the desired compound were recovered essentially as described in EXAMPLE 3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06881733B1
Source datasetuspto-grants-2005_04
ORD IDord-25c0608edb564a4289cc27a17156d41d
Source noteuspto-grants-2005_04