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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 942생성일: 2026년 10월 23일

3,4,4-Trifluorobut-3-en-1-ol → 3,4,4-Trifluoro-3-butenoic acid

https://huagongshe.com/ko/reaction/942

반응식

참여 물질

역할이름HCID투입량
반응물3,4,4-Trifluorobut-3-en-1-olHCID 11768573—
반응물Jones' reagentHCID 131709961—
용매AcetoneHCID 180—
생성물3,4,4-Trifluoro-3-butenoic acidHCID 15239174—

반응 단계

The first method involves hydrolysis of 4-bromo-1,1,2-trifluoro-1-butene (II) with water in the presence of N-methyl pyrrolidinone to give 3,4,4-trifiuoro-3-buten-1-ol (III), followed by Jones oxidation under conditions not previously known. These conditions are at a temperature of about 51°-54° C. In addition, the 3,4,4-trifluoro-3-buten-1-ol in acetone solvent and the Jones reagent are added to the reaction vessel simultaneously to afford 3,4,4-trifluoro-3-butenoic (IV) acid in 52% overall yield. ##STR4##

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723470
출처 데이터셋uspto-grants-1998_03
ORD IDord-e35af9d11de64be984c69f790192129f
출처 메모uspto-grants-1998_03