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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2063243Generated: October 29, 2026

Ethyl Acetate → HCID 57638733, compound

https://huagongshe.com/reaction/2063243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantTrimethylsilyl triflateHCID 65367—
ReactantHCID 5256039HCID 5256039—
ReactantHCID 18717149HCID 18717149—
ReactantHCID 178418361HCID 178418361—
SolventDichloromethaneHCID 6344—
ProductHCID 57638733HCID 57638733100%

Reaction Conditions

Temperature-5 °C

Reaction Steps

A clean oven dried flask was charged with the 6-(4-nitro-phenyl)-hexane-2,4-dione (3.7 g, 15.72 mmol), dry CH2Cl2 (20 ml) followed by bisTMS ethylene glycol (38.5 ml, 157.3 ml) were added to the flask and the resulting solution was cooled to −5° C. with stirring under argon. TMSOTf (300 μl ) was added to the reaction mixture and the solution was stirred at −5° C. for 6 h. Reaction was quenched with pyridine (10 ml) and poured into sat. NaHCO3. The mixture was extracted with EtOAc and the organic layer was washed with water, brine, dried (Na2SO4) and concentrated to give a yellow solid. The solid was triturated with hexanes to give a free flowing pale yellow solid (3.5 g, 72%) which was dissolved in EtOAc (50 ml) and hydrogenated on a Parr shaker starting with 50 psi of hydrogen pressure. After two hours the reaction was filtered through a pad of celite, the celite was washed thoroughly with CH2Cl2/MeOH and combined organics were concentrated to give title compound (1.46 g, 100%) as an oil that solidifies upon standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288349B2
Source datasetuspto-grants-2012_10
ORD IDord-f19aac928f1d4b81b333518da79ac890
Source noteuspto-grants-2012_10