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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066919Generated: November 1, 2026

Ethyl Acetate → Ethyl 2-hydroxy-4-methyl-2-(trifluoromethyl)pent-4-enoate

https://huagongshe.com/reaction/1066919

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantAmmonium ChlorideHCID 25517—
Reactant3-Bromo-2-methyl-1-propeneHCID 357785—
ReactantEthyl 3,3,3-trifluoro-2-oxopropanoateHCID 2737239—
CatalystManganeseHCID 23930—
CatalystZincchlorideHCID 3007855—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-hydroxy-4-methyl-2-(trifluoromethyl)pent-4-enoateHCID 17935595—

Reaction Conditions

Temperature0 °C

Reaction Steps

1.3 g of anhydrous zinc chloride and 13.2 g of granular manganese are heated to boiling in 100 ml of tetrahydrofuran and boiled with 0.2 ml of methallyl bromide for 30 minutes. Then, the solution of 25 g of methallyl bromide and 17 g of trifluoropyruvic acid ethyl ester in 80 ml of tetrahydrofuran is added in drops at boiling heat over 2 hours, and boiled for another hour. Then, while being cooled with ice, saturated ammonium chloride solution and 300 ml of ethyl acetate are added, stirred for 30 minutes at 0° C., and the separated ethyl acetate phase is washed with saturated ammonium chloride solution and three times with water. The solvent is dried (Na2SO4) and concentrated by evaporation, and the residue is distilled in a vacuum. 17.6 g of 2-hydroxy-4-methylene-2-trifluoromethyl-valeric acid ethyl ester, boiling point 48° C./1 hPa, is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06245804B1
Source datasetuspto-grants-2001_06
ORD IDord-e13108e1b649471bb1f905af5e790610
Source noteuspto-grants-2001_06