Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420900Generated: October 31, 2026

Sodium Acetate → 1,2,6,7-Tetrahydro-8H-indeno[5,4-b]furan-8-one

https://huagongshe.com/reaction/420900

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AcetateHCID 517045—
Reactant4,5-Dibromo-1,2,6,7-tetrahydro-8H-indeno[5,4-b]furan-8-oneHCID 11727281—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product1,2,6,7-Tetrahydro-8H-indeno[5,4-b]furan-8-oneHCID 1113761686.6%

Reaction Steps

4,5-Dibromo-1,2,6,7-tetrahydro-8H-indeno[5,4-b]furan-8-one (280 kg, 843 mol), anhydrous sodium acetate (173 kg, 2109 mol), methanol (6384 L) were mixed, and the reaction system was replaced with nitrogen. Then, to the reaction mixture was added 10% Pd/C (30.8 kg, as dry weight), and pressurized with hydrogen to 0.29 to 0.49 MPa, and catalytically reduced at about 40° C. for 8 hrs with stirring at such a stirring rate that the gas-liquid overall mass transfer coefficient KLa(1/hr) is about 15. The catalyst was filtered, and the filtrate was concentrated under reduced pressure, and further water was added to the residue, followed by concentrating under reduced pressure to substitute the solvent, cooling and stirring for 1 hr to mature. The crystallization solution was filtered to give wet crystals of title compound (amount 127 kg as dry weight, yield 86.6%). The content of dimer in the wet crystals was less than 0.1% by weight. (2) Purification Step

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08097737B2
Source datasetuspto-grants-2012_01
ORD IDord-c70c8df87e32428fbe516f9630772ea8
Source noteuspto-grants-2012_01