HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Bis(diphenylphosphino)butane → HCID 90067224, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Bis(diphenylphosphino)butane | HCID 82124 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 118413229 | HCID 118413229 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 90067224 | HCID 90067224 | — |
Reaction Steps
A 4 mL vial was charged with palladium(II) acetate (2.6 mg, 0.012 mmol), 1,4-bis(diphenylphosphino)butane (3.0 mg, 7.03 μmol), and ethanol (0.1 ml). This catalyst mixture was degassed (3×) and stirred under nitrogen for 15 min. Sodium borohydride (3.5 mg, 0.093 mmol) was added to a stirred solution of (3R,3aR,6R,6aR)-6-[1-allyl-6-chloro-5-[4-[5-(2,2,2-trifluoroethyl)-4,6-dihydropyrrolo[3,4-c]pyrazol-2-yl]phenyl]imidazo[4,5-b]pyridin-2-yl]oxy-2,3,3a,5,6,6a-hexahydrofuro[3,2-b]furan-3-ol (9.5 mg, 0.016 mmol) in ethanol (0.15 ml) and DCM (0.05 ml). The sodium borohydride mixture was degassed (3×) and placed under nitrogen. The catalyst mixture was transferred via syringe to the sodium borohydride reaction mixture.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09290517B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-dd53a50fc00b4b6baa359f5a048b51ad |
| Source note | uspto-grants-2016_03 |