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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366927Generated: October 25, 2026

Water → Ethyl 2-methyl-4,4,4-trifluoroacetoacetate

https://huagongshe.com/reaction/366927

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl 4,4,4-trifluoroacetoacetateHCID 67793—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventSodium chloride; waterHCID 57417360—
ProductEthyl 2-methyl-4,4,4-trifluoroacetoacetateHCID 2737204—

Reaction Steps

Sodium hydride (7.05 g of a 50% oil dispersion, 0.15 mol) was washed 3 times with 25 ml of dimethoxyethane to remove the oil and then suspended in 220 ml of dimethoxyethane, under an argon atmosphere and cooled in an ice bath. A solution of ethyl 3-keto-4,4,4-trifluorobutanoate (25.77 g, 0.14 mol) in 25 ml of dimethoxyethane was added dropwise from an addition funnel to the stirred suspension. After the addition was completed, the cooling bath was removed and the reaction mixture stirred for 30 minutes past the cessation of hydrogen gas evolution. Methyl iodide (43.0 ml, 0.70 mole) was added by syringe and the reaction mixture refluxed overnight. The reaction was cooled to room temperature and poured into a separatory funnel containing a 1:1:1 mixture of saturated ammonium chloride:brine:water. The layers were separated and the aqueous phase extracted with 100 ml ether. The combined organic phase and ether extract was washed with brine, dried over magnesium sulfate and filtered. The solvents were removed by distillation at atmospheric pressure using a Vigreaux column leaving ethyl 3-keto-2-methyl-4,4,4-trifluorobutanoate as the pot residue. Rf: (EtAc/hexane--20:80)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06130315
Source datasetuspto-grants-2000_10
ORD IDord-8b38f0d4a0884ecab3785df05befd069
Source noteuspto-grants-2000_10