HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 6-Methoxy-4-(4,4,4-trifluoro-butyl)-isoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium peroxide | HCID 14803 | — |
| Reactant | 1,1,1-Trifluoro-4-iodobutane | HCID 2775189 | — |
| Reactant | 6-Methoxyisoquinoline | HCID 11040978 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-Methoxy-4-(4,4,4-trifluoro-butyl)-isoquinoline | HCID 57647053 | 30.4% |
Reaction Steps
2 g 6-Methoxy-isoquinoline were dissolved in 25 mL of dry tetrahydrofuran. 12.56 mL of a 1 M solution of potassium triethyl borohydrate were added dropwise. The solution was allowed to stir at room temperature for 2 h, then 3.29 g of 4,4,4-Trifluoro-1-iodobutane were added dropwise. The solution was allowed to stir overnight, then 32 mL of 1M sodium hydroxide and 12 mL of sodium peroxide solution (35%) were added. Stirring was continued for another 3 hrs, then the solution was diluted with dichloromethane, extracted with water and brine and the organic layer was dried over sodium sulfate and evaporated to dryness. Silica gel chromatography yields 1.03 g of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08722671B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-578f06296ec841fd9fd8fe9cf661762b |
| Source note | uspto-grants-2014_05 |