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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424935Generated: October 25, 2026

Ethyl trifluoroacetate → 2,2,2-Trifluoro-1-(2-methyl-1,3-dithian-2-yl)ethanone

https://huagongshe.com/reaction/1424935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl trifluoroacetateHCID 9794—
Reactant2-Methyl-1,3-dithianeHCID 22329—
ReactantAmmonium ChlorideHCID 25517—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2,2,2-Trifluoro-1-(2-methyl-1,3-dithian-2-yl)ethanoneHCID 8664848042.3%

Reaction Conditions

Temperature-20 °C

Reaction Steps

2-Methyl-1,3-dithiane (1.50 g, 11.2 mmol) was dissolved in THF (50 mL), followed by cooling to −20° C. Then, n-butyllithium (1.58 M solution in hexane, 7 mL, 11.1 mmol) was added dropwise and the mixture was stirred for two hours. Ethyl trifluoroacetate (1.4 mL, 11.8 mmol) was added, and the mixture was heated to room temperature and stirred for 20 hours. Aqueous ammonium chloride solution was added to the reaction solution, followed by extraction with ethyl acetate. Then, the organic layer was washed with brine and dried over anhydrous sodium sulfate. Following concentration under reduced pressure, the residue was purified by silica gel column chromatography (elution solvent: hexane/ethyl acetate=100/0, 95/5, 85/15) to obtain 1.09 g of the title compound as a pale yellow solid (42%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927588B2
Source datasetuspto-grants-2015_01
ORD IDord-283fd3b819e94dec9d0a1a15f990748f
Source noteuspto-grants-2015_01