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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1785731Generated: October 31, 2026

Triphenylphosphine → HCID 68903790, compound

https://huagongshe.com/reaction/1785731

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Thiopheneboronic acidHCID 2733960—
ReactantHCID 68903769HCID 68903769—
Catalystpalladium(II) acetateHCID 167845—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68903790HCID 6890379073%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of aryl iodide (191) (100 mg, 0.19 mmol), 2-thiopheneboronic acid (48 mg, 0.38 mmol), palladium acetate (4 mg, 0.019 mmol) and triphenylphosphine (10 mg, 0.38 mmol) in tetrahydrofuran (10 mL) was added sodium bicarbonate (10 mL, saturated aqueous). The reaction mixture was heated to reflux (65° C.) for 4 h, cooled, filtered and partitioned between water (20 mL) and ethyl acetate (20 mL). The organic phase was separated and washed with brine (20 mL), dried (Na2SO4), filtered and the solvent removed under reduced pressure to afford the crude product, as a brown oil. Purification by silica gel chromatography (20% ethyl acetate/iso-hexane eluant) gave the title compound (193) as a brown solid (67.2 mg, 73% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504522B2
Source datasetuspto-grants-2009_03
ORD IDord-0cd42dda05e64188b4bc8d4b43d19fc1
Source noteuspto-grants-2009_03