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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1460282Generated: November 1, 2026

Ethyl trifluoroacetate → HCID 19983612, compound

https://huagongshe.com/reaction/1460282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl trifluoroacetateHCID 9794—
Reactant1-[(2-Methylbut-3-yn-2-yl)oxy]-4-(trifluoromethoxy)benzeneHCID 15052917—
ReactantDiethylether hexaneHCID 21584099—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19983612HCID 19983612—

Reaction Steps

To a solution of 1.47 g (6 mmol) of 1-(1,1-dimethyl-2-propynyloxy)-4-trifluoromethoxybenzene in 25 ml of tetrahydrofuran cooled to -78° C. is added 2.4 ml of n-butyllithium (2.5M in hexanes). The solution is maintained with stirring for 1 hour. The mixture is treated with 1.70 g (12 mmol, 1.43 ml) of ethyl trifluoroacetate at -78° C. and is allowed to warm to room temperature. After stirring for 1 hour, the mixture is diluted with water and is extracted with ethyl ether (3 times). The combined ethereal extracts are washed with aqueous sodium bicarbonate, dried over magnesium sulfate, filtered and evaporated to give a light oil. Flash chromatography using hexane:ethyl ether (65:35) affords the title compound: IR (film) 2215, 1740 cm-1 ; NMR (CDCl3) δ1.73 (6H, s), 7.16 (4H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05070207
Source datasetuspto-grants-1991_12
ORD IDord-94dacfd66d4e478984425bd4977019b9
Source noteuspto-grants-1991_12