Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Acetone → 6-Methyl-2-heptanone
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Acetone | HCID 180 | — |
| 반응물 | 3-Methylbutanal | HCID 11552 | — |
| 생성물 | 6-Methyl-2-heptanone | HCID 13572 | — |
반응 단계
To aid comprehension, the reaction will be explained here by the example of the reaction of acetone with isovaleraldehyde to produce 6-methylheptan-2-one. The reaction takes place “in situ” via the stage of aldol condensation with the formation of the corresponding β-hydroxyketone, which is not isolated. Dehydration to 6-methylhept-3-en-2-one takes place under the reaction conditions, and this is hydrogenated selectively to the corresponding methylketone with the hydrogenation catalyst distributed homogeneously in the aqueous catalyst phase.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06583323B2 |
| 출처 데이터셋 | uspto-grants-2003_06 |
| ORD ID | ord-f282adfabe8d45cda6642831763bf31f |
| 출처 메모 | uspto-grants-2003_06 |