Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
3,4,4-Trifluorobut-3-en-1-ol → 3,4,4-Trifluoro-3-butenoic acid
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 3,4,4-Trifluorobut-3-en-1-ol | HCID 11768573 | — |
| 반응물 | Jones' reagent | HCID 131709961 | — |
| 용매 | Acetone | HCID 180 | — |
| 생성물 | 3,4,4-Trifluoro-3-butenoic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05723470 |
| 출처 데이터셋 | uspto-grants-1998_03 |
| ORD ID | ord-e35af9d11de64be984c69f790192129f |
| 출처 메모 | uspto-grants-1998_03 |