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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404651Generated: October 30, 2026

2,2'-Bipyridine → HCID 46911037, compound

https://huagongshe.com/reaction/1404651

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2'-BipyridineHCID 1474—
ReactantBorohydrideHCID 28123—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86645080HCID 86645080—
CatalystCobalt(II) chlorideHCID 24288—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 46911037HCID 4691103759%

Reaction Conditions

Temperature0 °C

Reaction Steps

5-{4-[2-(3-chlorophenyl)-2-hydroxyethoxy]benzylidene}-1,3-thiazolidine-2,4-dione (0.74 g, 2.00 mmol) was dissolved in THF (20 mL). Water (20 mL) was added and then more THF was added until all solids dissolved. A small crystal of cobalt chloride was added, followed by 2,2′-bipyridine (69 mg, 0.44 mmol). The reaction mixture was cooled to 0° C. NaBH4 was added in portions until the blue color persisted. The color gradually faded and was regenerated repeatedly by small additions of borohydride and HOAc. When HPLC indicated that the reaction was complete, the reaction mixture was partitioned between EtOAc and H2O. HOAc was added until the pH of the aqueous phase was ca. 6, and then the aqueous phase was extracted with EtOAc. The combined organic phases were washed with brine, dried (Na2SO4), filtered and evaporated in vacuo. The residue was chromatographed on a small silica gel column eluting with 0-10% EtOAc/DCM. Fractions containing product were combined and evaporated in vacuo to give 0.44 g (59%) of a sticky yellow solid. MS (ESI−) for C18H16ClNO4S m/z 376.1 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912335B2
Source datasetuspto-grants-2014_12
ORD IDord-31a7d28689f045ca9df26c7477079863
Source noteuspto-grants-2014_12