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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 965938Generated: October 25, 2026

2-(4-Oxo-3,4-dihydro-2H-pyran-2-ylmethyl)-isoindole-1,3-dione → 2-(4-Oxo-tetrahydro-pyran-2-ylmethyl)-isoindole-1,3-dione

https://huagongshe.com/reaction/965938

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Oxo-3,4-dihydro-2H-pyran-2-ylmethyl)-isoindole-1,3-dioneHCID 21936668—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product2-(4-Oxo-tetrahydro-pyran-2-ylmethyl)-isoindole-1,3-dioneHCID 2193678787%

Reaction Steps

2-(4-Oxo-3,4dihydro-2H-pyran-2-ylmethyl)-isoindole-1,3-dione (13 g, 0.051 mol) was dissolved in ethyl acetate (250 ml) and placed in a Parr bottle. 10% Pd/C (1.5 g) was carefully added and the mixture was shaken under a pressure of 30 psi of hydrogen for 6.5 h (Parr apparatus). Filtration followed by evaporation of the ethyl acetate in vacuo afforded a crude 11.5 g of 2-(4-oxo-tetrahydro-pyran-2-ylmethyl)-isoindole-1,3-dione pure enough for the next step. Analytical pure compound could be obtained by purification of a small sample (250 mg) by column chromatography on silica gel, utilising a mixture of hexane/ethyl acetate as a gradient (from 100/0 to 50/50). Pure fractions were collected and the solvent evaporated in vacuo affording 142 mg (55%) of 2-(4-oxo-tetrahydro-pyran-2-ylmethyl)-isoindole-1,3-dione as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06951878B2
Source datasetuspto-grants-2005_10
ORD IDord-a4bccce14247485f901151a1e04f0a16
Source noteuspto-grants-2005_10