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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368893Generated: October 31, 2026

Hydrochloric Acid → 1,2,3,4-Tetrahydrobenzo-furo[3,2-c]pyridine hydrochloride

https://huagongshe.com/reaction/1368893

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantO-Phenylhydroxylamine hydrochlorideHCID 6365179—
Reactant4,4-Piperidinediol, hydrochlorideHCID 11636836—
SolventIsopropanolHCID 3776—
Product1,2,3,4-Tetrahydrobenzo-furo[3,2-c]pyridine hydrochlorideHCID 1249951364.1%

Reaction Conditions

Temperature20 °C

Reaction Steps

A mixture of O-phenylhydroxylamine hydrochloride (1:1) (0.625 mol) and 4,4-piperidinediol hydrochloride (1:1) (0.682 mol) in 2-propanol (615 ml) was stirred at 20° C. HCl (353 ml) was added dropwise at 20° C. The reaction mixture was gently heated to reflux temperature. The reaction mixture was stirred and refluxed for 3 hours, then cooled to room temperature. The precipitate was filtered off, washed with diisopropyl ether, and dried. This fraction was crystallized from water (1600 ml). The desired compound was allowed to crystallize out while stirring. The precipitate was filtered off, washed with 2-propanol and diisopropyl ether, then dried, yielding 84 g (64%) of 1,2,3,4-tetrahydrobenzo-furo[3,2-c]pyridine hydrochloride (1:1)(interm. 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06576640B1
Source datasetuspto-grants-2003_06
ORD IDord-4fc769f77170436dafbe41d3dd892209
Source noteuspto-grants-2003_06