HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethyloxonium tetrafluoroborate → HCID 21495341, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethyloxonium tetrafluoroborate | HCID 2723982 | — |
| Reactant | HCID 21495275 | HCID 21495275 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21495341 | HCID 21495341 | — |
Reaction Steps
A solution of triethyloxonium fluoroborate (3.5 g) and the amide of formula X, N,1-dimethyl-1,3,4,9-tetrahydroindeno[2,1-c]pyran-1-propionamide (5.5 g), described in Example 108, in 100 ml of methylene chloride is evaporated at reduced pressure and the residue dissolved in 50 ml of absolute ethanol. Sodium borohydride (1.35 g) is added in portions to the stirred solution at 0° C. When the addition is complete, stirring is continued for 18 hr. at 25° C. The solution is poured into 250 ml of water and extracted with 3 × 30 ml portions of ether. The combined extracts are washed with water, dried (MgSO4) and evaporated yielding the title compound, identical to the product of Example 285.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03995052 |
| Source dataset | uspto-grants-1976_11 |
| ORD ID | ord-5042efa4ccc6488a8422fc4bf2e32da5 |
| Source note | uspto-grants-1976_11 |