Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432672Generated: October 30, 2026

Water → 4-Benzyl-3-hydroxy-3,4-dihydro-1-isoquinolinone

https://huagongshe.com/reaction/432672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant4-BenzylidenehomophthalimideHCID 131724257—
SolventMethanolHCID 887—
Product4-Benzyl-3-hydroxy-3,4-dihydro-1-isoquinolinoneHCID 18760246—

Reaction Steps

Sodium borohydride (1.2 g, 32 mmol) was added in portions to a stirred suspension of 4-benzylidenehomophthalimide (2 g, 8 mmol) in methanol (50 ml), then the stirred mixture was heated under reflux for 4 hours, cooled to ambient temperature and added to water (200 ml). The product was extracted into ethyl acetate (3×50 ml), the combined extracts were washed with water (2×30 ml), dried (MgSO4) and the solvent was removed in vacuo. The residue was dissolved in the minimum volume of ether and sufficient hexane was added to precipitate the product. The resulting solid was collected by filtration, washed with hexane (20 ml) and dried in vacuo to give the 4-benzyl-3-hydroxy-3,4-dihydro-1-isoquinolinone intermediate which was used without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06664269B2
Source datasetuspto-grants-2003_12
ORD IDord-cbdc28dc43ce4b18b5de0d1999055ba9
Source noteuspto-grants-2003_12