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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1060985Generated: October 30, 2026

4-Bromodiphenyl Ether → HCID 22600006, compound

https://huagongshe.com/reaction/1060985

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromodiphenyl EtherHCID 7565—
ReactantAmmonium ChlorideHCID 25517—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantHCID 178419636HCID 178419636—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22600006HCID 2260000645%

Reaction Steps

To an 100 ml tetrahydrofuran solution of 3.5 g of N-tert-butoxycarbonyl-4-piperidone, a 35 ml of 4-phenoxyphenyl magnesium bromide prepared from 4-bromodiphenyl ether (0.6 mol/l tetrahydrofuran solution) was dropwise added under ice cooling and the resultant mixture was stirred for 1 hour. To the reaction mixture was added a 30 ml of saturated aqueous ammonium chloride solution. The product was extracted with ether. The extract was washed with saturated saline, dried, filtered, then concentrated under reduced pressure to give a residue, which was then purified by silica gel column chromatography (hexane:ethyl acetate=3:1) to give N-tert-butoxycarbonyl-4-(4-phenoxyphenyl)-4-piperidinol in an amount of 2.92 g (yield 45%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06525199B1
Source datasetuspto-grants-2003_02
ORD IDord-5500bcd7baae4c94beac6f65950f71d9
Source noteuspto-grants-2003_02