Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 263459Generated: November 2, 2026

Hydrochloric Acid → 5-Chloro-3-(1-methyl-4-piperidyloxy)-1,2-benzisoxazole hydrochloride

https://huagongshe.com/reaction/263459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant5-Chloro-3-(1-methyl-4-piperidyloxy)-1,2-benzisoxazoleHCID 19038087—
SolventEthanolHCID 702—
Solvent1,4-DioxaneHCID 31275—
Product5-Chloro-3-(1-methyl-4-piperidyloxy)-1,2-benzisoxazole hydrochlorideHCID 19038116197.7%

Reaction Steps

A solution of 2.20 g (8.24 mmole) of 5-chloro-3-(1-methyl-4-piperidyloxy)-1,2-benzisoxazole (prepared as described in Example 11) in 20 ml of ethanol was cooled to 5° C. 2.5 ml of a 4N solution of hydrogen chloride in dioxane were added dropwise to the cooled solution, and the resulting mixture was stirred at room temperature for 30 minutes. At the end of this time, the solvent was removed from the reaction mixture by distillation under reduced pressure. The solid residue thus obtained was recrystallized from ethanol to afford 2.47 g (yield 98.7%) of the title compound as colorless curd-like crystals, melting at 212°-214° C. (with decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05643923
Source datasetuspto-grants-1997_07
ORD IDord-c5107a3f6a814cd9816fcb7310da315e
Source noteuspto-grants-1997_07