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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1661401Generated: October 27, 2026

Acetone → 2-Methyl-7-(1-methylethylidene)-6,7-dihydro-8H-indeno[5,4-d][1,3]oxazol-8-one

https://huagongshe.com/reaction/1661401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantCyanogen iodideHCID 10478—
Reactant2-Methyl-6,7-dihydro-8H-indeno[5,4-d][1,3]oxazol-8-oneHCID 57781277—
SolventTetrahydrofuranHCID 8028—
Product2-Methyl-7-(1-methylethylidene)-6,7-dihydro-8H-indeno[5,4-d][1,3]oxazol-8-oneHCID 5778127033%

Reaction Conditions

Temperature50 °C

Reaction Steps

2-Methyl-6,7-dihydro-8H-indeno[5,4-d][1,3]oxazol-8-one (1.87 g, 10.0 mmol), acetone (3.68 mL, 50.0 mmol) and ICN Alumina B (manufactured by ICN, Akt.1, 20 g) were suspended in tetrahydrofuran (50 mL), and the mixture was stirred at 50° C. for 9 hr. Acetone (3.68 mL, 50.0 mmol) was added, and the mixture was further stirred for 12 hr. The reaction solution was filtered, and the filtrate was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane=10/90→50/50) to give the title compound (742 mg, yield 33%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030337B2
Source datasetuspto-grants-2011_10
ORD IDord-2dc00c06fd124a3eb56985a998ad17be
Source noteuspto-grants-2011_10