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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 962632Generated: October 30, 2026

3-Benzyl-8-methoxy-1,2,3,4-tetrahydro-chromeno[3,4-c]pyridin-5-one → 8-Methoxy-1,2,3,4-tetrahydro-chromeno[3,4-c]pyridin-5-one

https://huagongshe.com/reaction/962632

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Benzyl-8-methoxy-1,2,3,4-tetrahydro-chromeno[3,4-c]pyridin-5-oneHCID 9883587—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product8-Methoxy-1,2,3,4-tetrahydro-chromeno[3,4-c]pyridin-5-oneHCID 1313691849%

Reaction Steps

A solution of 3-benzyl-8-methoxy-1,2,3,4-tetrahydro-chromeno[3,4-c]pyridin-5-one (8.2 g, 26 mmol) in 150 mL of methanol and 100 mL of tetrahydrofuran is hydrogenated at room temperature over a palladium on carbon catalyst (0.85 g) for 18 hours. The catalyst is filtered and the filtrate evaporated. Recrystallization of the residue from acetonitrile with a small amount of added water gives 2.9 g (49%) of product; mp 179°-181° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05760050
Source datasetuspto-grants-1998_06
ORD IDord-103750842fdb4b3f96836dc4d4c5ba68
Source noteuspto-grants-1998_06