HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275742Generated: October 27, 2026
Hydrochloric Acid → 1,2,3,4-Tetrahydrobenzo-furo[3,2-c]pyridine hydrochloride
https://huagongshe.com/reaction/275742
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | O-Phenylhydroxylamine hydrochloride | HCID 6365179 | — |
| Reactant | 4,4-Piperidinediol, hydrochloride | HCID 11636836 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 1,2,3,4-Tetrahydrobenzo-furo[3,2-c]pyridine hydrochloride | HCID 12499513 | 64.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06352999B1 |
|---|
| Source dataset | uspto-grants-2002_03 |
|---|
| ORD ID | ord-78dcf7c3f9c04c82b22c8e4610fa32c3 |
|---|
| Source note | uspto-grants-2002_03 |
|---|