HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1460282Generated: November 1, 2026
Ethyl trifluoroacetate → HCID 19983612, compound
https://huagongshe.com/reaction/1460282
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl trifluoroacetate | HCID 9794 | — |
| Reactant | 1-[(2-Methylbut-3-yn-2-yl)oxy]-4-(trifluoromethoxy)benzene | HCID 15052917 | — |
| Reactant | Diethylether hexane | HCID 21584099 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19983612 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05070207 |
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| Source dataset | uspto-grants-1991_12 |
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| ORD ID | ord-94dacfd66d4e478984425bd4977019b9 |
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| Source note | uspto-grants-1991_12 |
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