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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,6-Trivinylboroxin-Pyridine ComplexHCID 2734806—
Reactant5-Bromo-3-methyl-2-[(propan-2-yl)oxy]pyridineHCID 22591177—
CatalystHCID 178418397HCID 178418397—
SolventDiethyl EtherHCID 3283—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventPotassium CarbonateHCID 11430—
ProductHCID 66933582HCID 6693358275.4%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598208B2
Source datasetuspto-grants-2013_12
ORD IDord-84e41ab838c5433fac864a53803f0e4c
Source noteuspto-grants-2013_12