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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929200Generated: October 31, 2026

1,4-Bis(diphenylphosphino)butane → HCID 90067224, compound

https://huagongshe.com/reaction/929200

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Bis(diphenylphosphino)butaneHCID 82124—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 118413229HCID 118413229—
Catalystpalladium(II) acetateHCID 167845—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductHCID 90067224HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290517B2
Source datasetuspto-grants-2016_03
ORD IDord-dd53a50fc00b4b6baa359f5a048b51ad
Source noteuspto-grants-2016_03