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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1985599Generated: October 26, 2026

1,2-Cyclooctanedione → (Z)-2-(4,4-dimethyl-2-oxo-pentyl)-cyclooct-2-enone

https://huagongshe.com/reaction/1985599

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-CyclooctanedioneHCID 543698—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant(4,4-Dimethyl-2-oxo-pentyl)-phosphonic acid dimethyl esterHCID 25112585—
Solventtert-ButanolHCID 6386—
Product(Z)-2-(4,4-dimethyl-2-oxo-pentyl)-cyclooct-2-enoneHCID 2511258622.5%

Reaction Steps

A solution of potassium tert-butoxide (0.192 g) in tert-butanol (10 mL) under an argon atmosphere was treated at 50° C. with (4,4-dimethyl-2-oxo-pentyl)-phosphonic acid dimethyl ester (0.38 g) and cyclooctane-1,2-dione (0,2 g), and the mixture was then heated at reflux for 12 h under an argon atmosphere. The reaction mixture was partitioned between water and AcOEt, the layers were separated, the aqueous layer extracted twice with AcOEt. The combined organic layers were washed with water, dried over Na2SO4, filtered and evaporated. The residue was purified by flash chromatography (heptane/AcOEt 100% to 95%) to give (Z)-2-(4,4-dimethyl-2-oxo-pentyl)-cyclooct-2-enone (0.076 g) as a light yellow oil. MS (ESI): 237.0 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07547697B2
Source datasetuspto-grants-2009_06
ORD IDord-0b4ec987d14549c0aa8e927d819d4736
Source noteuspto-grants-2009_06