HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 7-{4-[(2-Cyclopropyl-ethylamino)-methyl]-2-fluoro-phenoxy}-2,2-dimethyl-benzo[1,3]dioxin-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Cyclopropaneethanamine | HCID 10240761 | — |
| Reactant | 4-(2,2-Dimethyl-4-oxo-4H-benzo[1,3]dioxin-7-yloxy)-3-fluoro-benzaldehyde | HCID 57939035 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 7-{4-[(2-Cyclopropyl-ethylamino)-methyl]-2-fluoro-phenoxy}-2,2-dimethyl-benzo[1,3]dioxin-4-one | HCID 57939033 | — |
Reaction Steps
4-(2,2-Dimethyl-4-oxo-4H-benzo[1,3]dioxin-7-yloxy)-3-fluoro-benzaldehyde (I-1b-1: 24.8 g) and 2-cyclopropyl-ethylamine (6.2 g) were combined in 1,2-dichloroethane (1.0 L). After stirring at ambient temperature for 1 hour, sodium triacetoxyborohydride (83 g) was added to the solution. After stirring overnight, the reaction mixture was treated with an aqueous 2 N potassium hydroxide solution, the organic phase was separated, dried over magnesium sulfate, filtered, and evaporated to provide the title compound (I-1c-2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07618996B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-b85b557429544d5386ee15ba6575e40a |
| Source note | uspto-grants-2009_11 |