HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 44211738, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 44211737 | HCID 44211737 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 44211738 | HCID 44211738 | — |
Reaction Steps
(1-Butylpiperidin-4-ylmethyl)thiochroman-4-one-8-carboxylate (0.064 g, 0.177 mmol)(Example 2-1) was dissolved in ethanol (5 ml) and treated with sodium borohydride (0.007 g, 0.186 mmol) with stirring. After 3 h, the reaction mixture was evaporated under reduced pressure and the residue partitioned between CH2Cl2 and water. The aqueous layer was then extracted with CH2Cl2 and the combined organic extracts were dried (Na2SO4) and evaporated under reduced pressure to give the title compound as a pale yellow oil which was dried in vacuo (0.060 g, 93%) and subsequently converted to the oxalate salt. m.pt 147°-148° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05708174 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-45d9f804815f4f46ae7d23fb4d4adad0 |
| Source note | uspto-grants-1998_01 |