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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 14466Generated: October 26, 2026

7-Benzyloxy-3-(4-chlorophenyl)-2-isopropyl-8-methoxy-chromen-4-one → 3-(4-Chlorophenyl)-7-hydroxy-2-isopropyl-8-methoxy-chromen-4-one

https://huagongshe.com/reaction/14466

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Benzyloxy-3-(4-chlorophenyl)-2-isopropyl-8-methoxy-chromen-4-oneHCID 68703258—
CatalystHCID 178418390HCID 178418390—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product3-(4-Chlorophenyl)-7-hydroxy-2-isopropyl-8-methoxy-chromen-4-oneHCID 11602640—

Reaction Steps

A suspension of 7-benzyloxy-3-(4-chlorophenyl)-2-isopropyl-8-methoxy-chromen-4-one (2.68 g, 6.16 mmol) and Pd/carbon (20%, 268 mg) in tetrahydrofuran (30 ml), absolute ethanol (30 ml) and 5M HCl solution (15 ml) is stirred under a balloon of H2 at room temperature for 3 h. The reaction mixture is filtered through a pad of Celite filter aid, which is itself washed with tetrahydrofuran. The solvent is removed under reduced pressure to afford the desired product, which is used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732435B2
Source datasetuspto-grants-2010_06
ORD IDord-f6ceb956a24d4e769e39b92cd6f2fd8c
Source noteuspto-grants-2010_06