HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1159017Generated: October 31, 2026
2-(Tributylstannyl)furan → HCID 68689144, compound
https://huagongshe.com/reaction/1159017
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(Tributylstannyl)furan | HCID 4393688 | — |
| Reactant | HCID 16115648 | HCID 16115648 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 68689144 | HCID 68689144 | — |
Reaction Steps
To a degassed solution of tetrakis(triphenylphosphine)palladium(0) (3 mg, 0.002 mmol) in toluene (2 mL) was added N-(t-butoxycarbonyl)-(R)-1,3,4,10b-tetrahydro-9-bromo-7-trifluoromethyl-pyrazino[2,1-a]isoindol-6(2H)-one (50 mg, 0.12 mmol). The resulting solution was degassed by exposure to vacuum and then an argon atmosphere (×3). To this solution was added 2-(tributylstannyl)furan (0.038 mL, 0.12 mmol). The resulting solution was degassed a final time and was then warmed to reflux conditions. The light yellow solution was maintained at reflux conditions for 14 h and became gray in color. The reaction was cooled, diluted with ethyl acetate, aqueous hydrogen chloride (1N), and saturated aqueous sodium chloride. The layers were separated and the aqueous layer washed with ethyl acetate. The combined organic layers were dried over sodium sulfate, filtered, and concentrated. The resulting residue was purified by radial chromatography (10-30% ethyl acetate in hexanes) to give the desired product as a clear residue (44 mg, 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07812024B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-792ab4d522694992895984d4a1877d74 |
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| Source note | uspto-grants-2010_10 |
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