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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735470Generated: November 1, 2026

HCID 11808972, compound → HCID 12704136, compound

https://huagongshe.com/reaction/1735470

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05536716
Source datasetuspto-grants-1996_07
ORD IDord-78afe80a288243008e7dd902571b8a80
Source noteuspto-grants-1996_07