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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260589Generated: November 3, 2026

Ethyl Acetate → HCID 67081796, compound

https://huagongshe.com/reaction/1260589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant1-methoxy-4-(trimethylsilyl)-3-Butyn-2-oneHCID 85860021—
ReactantHCID 178418630HCID 178418630—
SolventDiethyl EtherHCID 3283—
ProductHCID 67081796HCID 6708179651%

Reaction Steps

52.85 ml of 0.5 M cyclopropylmagnesium bromide (26.43 mmol, Aldrich) are added to a solution of 3 g of 1-methoxy-4-(trimethylsilyl)but-3-yn-2-one (17.62 mmol) in 160 ml of ether. The mixture is stirred at ambient temperature overnight and is then cooled with a water/ice bath and a solution of NH4Claq and ethyl acetate is added. The mixture is extracted 3 times with ethyl acetate and the organic phases are then combined, dried over sodium sulphate, filtered, and concentrated under vacuum. The oily residue is purified by silica column chromatography, elution being carried out with a cyclohexane:ethyl acetate gradient, 100:0 to 80:20, so as to obtain 1.9 g of (±)-2-cyclopropyl-1-methoxy-4-(trimethylsilyl)but-3-yn-2-ol in the form of an oil, with a yield of 51%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470847B2
Source datasetuspto-grants-2013_06
ORD IDord-06c145b62af446589c20bc403f0255fd
Source noteuspto-grants-2013_06