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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266891Generated: October 31, 2026

HCID 11808972, compound → HCID 12704136, compound

https://huagongshe.com/reaction/266891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 11808972HCID 11808972—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 12704136HCID 1270413698.5%

Reaction Steps

To a suspension of 10% palladium on carbon (5 mg) in ethanol (5 mL) was added of 1'-benzylspiro[3H-2-benzopyran-3,4'-piperidine]-1(4H)-one (20 mg, 0.058 mmol). (Hashigaki et al Chem. Pharm. Bull. 32 pg 3561-3568 (1984)). Hydrogenation was performed at 1 atmosphere pressure at room temperature. The reaction was stirred for 2 hours under hydrogen atmosphere, until TLC analysis indicated that the reaction was complete. The catalyst was removed by vacuum filtration through celite 545 and the filtrate was concentrated to give the desired product (12.4 mg, 98.5%). FAB-MS calc. for C13H15NO2 217; found 218 (M+H, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05652235
Source datasetuspto-grants-1997_07
ORD IDord-f0d66afecfc443a1877d44c80a82706b
Source noteuspto-grants-1997_07