Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Acetate → 2-Acetyl-4,4-dimethyl-1,3-cyclohexanedione
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Acetate | HCID 175 | — |
| 반응물 | Acetone Cyanohydrin | HCID 6406 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 4-Nitrophenyl Acetate | HCID 13243 | — |
| 반응물 | 1,3-Cyclohexanedione, 4,4-dimethyl- | HCID 136360 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 2-Acetyl-4,4-dimethyl-1,3-cyclohexanedione | HCID 22648327 | — |
반응 단계
A 50-mL single neck round bottom flask was charged with 4-nitrophenyl acetate (2.03 g, 11.2 mmol), 4,4-dimethyl-1,3-cyclohexanedione (2.10 g, 15 mmol) and acetonitrile (15 mL). Then triethylamine (2.5 g, 25 mmol) and acetone cyanohydrin (0.14 mL, 1.5 mmol) were added and the mixture was stirred for 2 hours at ambient temperature. NMR analysis of an aliquot showed that 43% of the starting acetate was still unreacted. The mixture was then refluxed for 2 hours after which time NMR analysis of an aliquot showed no starting acetate remaining.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06809206B2 |
| 출처 데이터셋 | uspto-grants-2004_10 |
| ORD ID | ord-b34dc7bdba6e4b3cb799809b55c73a42 |
| 출처 메모 | uspto-grants-2004_10 |