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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1627414Generated: November 1, 2026

Water → HCID 67289237, compound

https://huagongshe.com/reaction/1627414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactantmethyl 6-chloropyrimidine-4-carboxylateHCID 245927—
Reactant2,4,6-Trivinylboroxin-Pyridine ComplexHCID 2734806—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventAcetonitrile--water (1/1)HCID 18373917—
ProductHCID 67289237HCID 6728923734%

Reaction Steps

Tetrakis-(triphenylphosphine)palladium(0) (0.40 g, 5 mol %) was added to a solution of methyl 6-chloropyrimidine-4-carboxylate (1.24 g) in DME (35 mL) and the solution left to stir at room temperature (20 min.). K2CO3 (1.11 g, 1.2 eq.), water (10 mL) and 2,4,6-trivinylcyclotriboroxane-pyridine complex (1.93 g, 1.2 eq.) were then added to the solution and the resultant mixture heated at reflux (24 hrs). The mixture was then cooled to room temperature and extracted with diethyl ether (200 mL) and the extract washed with water (30 mL). The diethyl ether extract was dried over MgSO4 and then diluted with hexane (200 mL). The solution was filtered through aluminium oxide (6 g) and the eluent concentrated in vacuo to give a yellow oil. The oil was then subjected to silica gel chromatography (10→100% EtOAc/Pet ether) followed by reverse phase (C18) chromatography (40% MeCN/water) to yield methyl 6-vinylpyrimidine-4-carboxylate as a white solid (0.40 g, 34% yield). 1H NMR, 270 MHz (CDCl3): 9.29 (d, 1H, H-2, J=1.1 Hz), 7.99 (d, 1H, H-5, J=1.1 Hz), dd, 1H, H-A, J=10.4 and 17.3 Hz), 6.61 (dd, 1H, H—C, J=1.0 and 17.3 Hz), 5.81 (dd, 1H, H—B, J=1.0 and 10.4 Hz), 4.02 (s, 3H, —CH3). 13C NMR, 67.5 MHz (CDCl3): 164.79 (2C), 159.22 (2C), 134.71, 124.92, 117.71, 53.52. ESI-MS Expected for molecular ion C8H8N2O2=164.0586. Found M+H=165.0664.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785595B2
Source datasetuspto-grants-2014_07
ORD IDord-9bc22fd843cf4f13b2bbb9c4079a1c53
Source noteuspto-grants-2014_07