HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1785731Generated: October 31, 2026
Triphenylphosphine → HCID 68903790, compound
https://huagongshe.com/reaction/1785731
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Thiopheneboronic acid | HCID 2733960 | — |
| Reactant | HCID 68903769 | HCID 68903769 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68903790 | HCID 68903790 | 73% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07504522B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-0cd42dda05e64188b4bc8d4b43d19fc1 |
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| Source note | uspto-grants-2009_03 |
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