HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 1-(3,4-Dimethoxyphenyl)butane-1,3-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Cyclohexane | HCID 8078 | — |
| Reactant | 3,4-Dimethoxyphenyl methyl ketone | HCID 14328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(3,4-Dimethoxyphenyl)butane-1,3-dione | HCID 368060 | — |
Reaction Steps
3.9 g of sodium hydride were initially introduced into 150 ml of cyclohexane, and a solution of 15 g of 1-(3,4-dimethoxyphenyl)ethanone in 16.3 ml of ethyl acetate was added. The reaction solution was boiled at 80° C. for 1 h, after which acetic acid was added and the whole was extracted with MTB-ether. The MTB-ether phase was dried over magnesium sulfate and subjected to rotary evaporation. The residue was chromatographed through silica gel (ethyl acetate/heptane 1/6). The following was obtained: 41 C12H14O4 (222.24); MS (ESI) 223 (M+H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07132428B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-744a70eef3984d2fb590d3ed12233ef3 |
| Source note | uspto-grants-2006_11 |