HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2281318Generated: November 2, 2026
Dichloromethane → 5-Ethenyl-2-(tetrazol-1-yl)pyridine
https://huagongshe.com/reaction/2281318
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 5-Bromo-2-(tetrazol-1-yl)pyridine | HCID 4136542 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Ethenyl-2-(tetrazol-1-yl)pyridine | HCID 89545188 | — |
Reaction Steps
To a stirring solution of 5-bromo-2-(1H-tetrazol-1-yl)pyridine (1.0 g, 4.42 mmol), in EtOH (70 mL) were added bis[(diphenylphosphino)ferrocene]dichloropalladium(II), complex with dichloromethane (0.361 g, 0.442 mmol), potassium vinyl trifluoroborate (1.18 g, 8.85 mmol, 2 equiv.), triethylamine (1.23 mL, 8.85 mmol, 2 equiv), and water (0.5 mL). The reaction mixture was heated to reflux (90° C., oil bath). Upon completion as determined by reverse phase HPLC-MS (1-2 h) and TLC (eluent: 10% ethyl acetate in hexanes), the reaction was cooled to room temperature, and then was diluted with water and extracted with EtOAc. The combined organic layers were washed with brine and dried over MgSO4. The extracts were concentrated and chromatographed over a column of SiO2 (0-20% EtOAc/hexanes as eluent). Evaporation of the solvent yielded the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09139585B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-9d2ea2b837d646d497c30a2e4526045f |
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| Source note | uspto-grants-2015_09 |
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