HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 321934Generated: October 30, 2026
Tributylvinyltin → HCID 9840745, compound
https://huagongshe.com/reaction/321934
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributylvinyltin | HCID 81998 | — |
| Reactant | Tris(furan-2-yl)phosphane | HCID 521585 | — |
| Reactant | HCID 18396490 | HCID 18396490 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 9840745 | HCID 9840745 | 915.3% |
Reaction Steps
To a solution of 2′,3′-di-O-acetyl-5′-deoxy-5-iodocytidine (1.6 g, 3.66 mmol) in 10 ml DMF were added Pd2(dba)3 (67 mg, 0.073 mmol) and tri-2-furylphosphine (85 mg, 0.366 mmol) and tri-n-butyl(vinyl)stannane (2.1 ml, 7.318 mmol ) under Ar atmosphere at room temperature. After stirring for 19 hours, tri-n-butyl(vinyl)stannane (2.1 ml, 7.318 mmol ) was added to the reaction mixture, and then the reaction mixture was warmed up to 40° C. with stirring for 24 hours. The solvent was removed in vacuo, and the residue was purified on a column of silica gel (eluent:ethyl acetate˜CH2Cl2:MeOH=95:5) to give 2′,3′-di-O-acetyl-5′-deoxy-5-vinylcytidine (1.13 g, 92%) as colorless solid:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06211166B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-46a69f882d254166abb7c22d608bb598 |
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| Source note | uspto-grants-2001_04 |
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