HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 22931945, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 14139907 | HCID 14139907 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methylamine | HCID 6329 | — |
| Product | HCID 22931945 | HCID 22931945 | 56.6% |
Reaction Steps
To a solution of 1.00 g of 4-(methoxymethoxy)-1-indanone in 10 ml of ethanol, 2.8 ml of 40% methylamine (methanol solution) and 367 mg of sodium cyanoborohydride were added. While stirring at room temperature, 0.55 ml of acetic acid was added dropwise and the mixture was heated at reflux for 4 hours. The reaction solution was air-cooled, combined with water and then extracted with ethyl acetate. After drying over anhydrous magnesium sulfate, the solvent was evaporated. The residue was purified by silica gel column chromatography to obtain 0.61 g of the desired compound as a deep green oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07205302B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-01c5d6db3c584a7ab9b40e3b9e3dfdc6 |
| Source note | uspto-grants-2007_04 |