HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 6-[(3-Phenylpropyl)amino]-1,3-benzoxazol-2(3H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Benzenepropanal | HCID 7707 | — |
| Reactant | 6-amino-1,3-benzoxazol-2(3H)-one | HCID 826989 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 6-[(3-Phenylpropyl)amino]-1,3-benzoxazol-2(3H)-one | HCID 14328078 | — |
Reaction Steps
To a suspension of 6-amino-2-benzoxazolone (6.00 g) and molecular sieves 4A (10.0 g) in dry benzene (100 ml) was added 3-phenylpropanal (5.25 ml), and then the mixture was stirred at room temperature for 1 hour. Methanol (150 ml) was combined with this and sodium borohydride (1.50 g) was added in portions at room temperature. The reaction mixture was filtered, the filtrate was concentrated and 5% sodium bicarbonate was added. The organic material was extracted with dichloromethane. The dichloromethane phase was separated, washed with brine. Drying and removal of solvent under reduced pressure gave a crude product which was crystallized from hot ethanol to afford 7.07 g of the title compound: mp 129°-130° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04835166 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-872f4d39c946407f88eda255ad017238 |
| Source note | uspto-grants-1989_05 |