HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908760Generated: October 28, 2026
2,4,6-Trivinylboroxin-Pyridine Complex → HCID 66933582, compound
https://huagongshe.com/reaction/1908760
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4,6-Trivinylboroxin-Pyridine Complex | HCID 2734806 | — |
| Reactant | 5-Bromo-3-methyl-2-[(propan-2-yl)oxy]pyridine | HCID 22591177 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Solvent | Potassium Carbonate | HCID 11430 | — |
| Product | HCID 66933582 | HCID 66933582 | 75.4% |
Reaction Steps
A solution of 5-bromo-2-isopropoxy-3-methyl-pyridine (1.24 g, 5.39 mmol) and 2,4,6-trivinylcyclotriboroxane pyridine complex (1.27 g, 5.26 mmol) in DME (12 mL) and 2 M aq. K2CO3 (5 mL) is degassed and put under argon before Pd(PPh3)4 (112 mg, 0.097 mmol) is added. The mixture is stirred at 80° C. for 15 h before it is cooled to rt, diluted with ether (50 mL), washed with sat. aq. NaHCO3 solution (2×30 mL), dried over MgSO4, filtered and concentrated. The crude product is purified by CC on silica gel eluting with heptane:EA 9:1 to give 2-isopropoxy-3-methyl-5-vinyl-pyridine (703 mg) as pale yellow oil; LC-MS: tR=1.01 min; [M+1]+=178.11.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08598208B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-84e41ab838c5433fac864a53803f0e4c |
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| Source note | uspto-grants-2013_12 |
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