HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 19600258, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Allylamine | HCID 7853 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 3-FURAN-3-YL-PROPIONALDEHYDE | HCID 11007893 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 19600258 | HCID 19600258 | — |
Reaction Steps
To a solution of the above crude 3-(3-furyl)propanal, 7.94 ml (106 mmol) of allylamine and 2.54 ml (42.3 mmol) of acetic acid in 100 ml of methanol, 1.33 g (21.2 mmol) of sodium cyanoborohydride was added at room temperature, followed by stirring at room temperature for 1 day. The reaction mixture was poured into aqueous sodium hydroxide and extracted with dichloromethane 3 times. The combined organic layer was dried over anhydrous magnesium sulfate; the solvent was distilled off under reduced pressure. The resulting crude product was purified by silica gel column chromatography (ethyl acetate to ethyl acetate/methanol=4/1) to yield the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05998433 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-554e7a6213e74b8da1d331b4b8c7bcc1 |
| Source note | uspto-grants-1999_12 |