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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389901Generated: October 31, 2026

Acetone → 7-(1-methylethylidene)-1,2,6,7-tetrahydro-8H-cyclopenta[d]furo[2,3-b]pyridin-8-one

https://huagongshe.com/reaction/2389901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantCyanogen iodideHCID 10478—
Reactant1,2,6,7-tetrahydro-8H-cyclopenta[d]furo[2,3-b]pyridin-8-oneHCID 59179368—
SolventTetrahydrofuranHCID 8028—
Product7-(1-methylethylidene)-1,2,6,7-tetrahydro-8H-cyclopenta[d]furo[2,3-b]pyridin-8-oneHCID 5917940172%

Reaction Steps

1,2,6,7-Tetrahydro-8H-cyclopenta[d]furo[2,3-b]pyridin-8-one (610 mg, 3.48 mmol), acetone (1.28 mL, 17.4 mmol) and ICN Alumina B (manufactured by ICN, Akt. 1, 10 g) were suspended in tetrahydrofuran (15 mL), and the suspension was stirred at room temperature for 3 hr. Acetone (1.28 mL, 17.4 mmol) was added, and the mixture was further stirred for 3 hr. The reaction solution was filtered, and the filtrate was evaporated under reduced pressure to give the title compound (539 mg, yield 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273761B2
Source datasetuspto-grants-2012_09
ORD IDord-43d626a53129413eabd316c960c677d8
Source noteuspto-grants-2012_09