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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 430460생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/430460

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Ammonium ChlorideHCID 25517—
반응물3-Bromo-2-methyl-1-propeneHCID 357785—
반응물Ethyl 3,3,3-trifluoro-2-oxopropanoateHCID 2737239—
촉매ManganeseHCID 23930—
촉매ZincchlorideHCID 3007855—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 2-hydroxy-4-methyl-2-(trifluoromethyl)pent-4-enoateHCID 17935595—

반응 조건

온도0 °C

반응 단계

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 methallylbromide and 17 g of trifluoropyruvic acid ethyl ester in 80 ml of tetrahydrofuran is added in drops at boiling heat over two hours and boiled for another hour. Then, it is added to saturated ammonium chloride solution and 300 ml of ethyl acetate while being cooled with ice, 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06323199B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-605ea9751b734934af7fb3bb1d09a996
출처 메모uspto-grants-2001_11