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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721593Generated: November 2, 2026

HCID 22413374, compound → HCID 22413368, compound

https://huagongshe.com/reaction/1721593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22413374HCID 22413374—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
ProductHCID 22413368HCID 22413368—

Reaction Steps

0.5 g (0.0016 mol) 1-(benzofuran-7-yl)-6,7-dihydroxy-3-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine was dissolved in a mixture of 25 ml ethanol and 2 ml acetic acid. 0.2 g catalyst (10% Pd/C) was added and the mixture was submitted to hydrogenation in a Parr apparatus at a pressure of 50 psi. After 24 h the catalyst was filtered off and the solution was concentrated in vacuo. The residue was redissolved in dichloromethane, the solution was washed subsequently with NaHCO3-solution, water and brine. Evaporation in vacuo gave 1-(2,3-dihydrobenzofuran-7-yl)-6,7-dihydroxy-3-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine as an offwhite foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05512562
Source datasetuspto-grants-1996_04
ORD IDord-e33998e8b3ff4e689efc0dc09604e428
Source noteuspto-grants-1996_04