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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858578Generated: November 4, 2026

HCID 54062527, compound → HCID 22128508, compound

https://huagongshe.com/reaction/1858578

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 54062527HCID 54062527—
CatalystZinc bromideHCID 10421208—
SolventDichloromethaneHCID 6344—
ProductHCID 22128508HCID 22128508101.7%

Reaction Steps

A solution of 280 mg (0.63 mmol) of tert-butyl (3RS,4RS)-3-(2,3-dihydro-benzo[1,4]dioxin-6-ylmethoxy)-4-(4-fluorophenyl)-piperidine-1-carboxylate in 5 ml of dry methylene chloride was treated with 808 mg (1.89 mmol) of anhydrous zinc bromide and the mixture was stirred at room temperature for 5 hours. Subsequently, the solvent was distilled off under reduced pressure, the residue was taken up in 10 ml of methanol, treated with 2 ml of 2N sodium hydroxide solution and the solid was separated. The filtrate was evaporated under reduced pressure and the residue was partitioned between methylene chloride and water. The organic phase was separated and evaporated under reduced pressure. There were obtained 220 mg (98% of theory) of (3RS,4RS)-3-(2,3-dihydrobenzo[1,4]dioxin-6-yl-methoxy)-4-(4-fluorophenyl)-piperidine as a yellowish solid; MS: 344 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06150526
Source datasetuspto-grants-2000_11
ORD IDord-a041aa7b316e4b2a8c6499e5878704f9
Source noteuspto-grants-2000_11