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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1481371Generated: October 30, 2026

5-Bromo-2-methylpyrimidine → 2-Methyl-5-vinylpyrimidine

https://huagongshe.com/reaction/1481371

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-2-methylpyrimidineHCID 14387744—
ReactantTri(butyl)vinyltinHCID 53438229—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solventtetrahydrofuran N,N-dimethylformamideHCID 21974620—
Product2-Methyl-5-vinylpyrimidineHCID 66848351—

Reaction Conditions

Temperature120 °C

Reaction Steps

The title compound was prepared by following general procedure 2. 5-Bromo-2-methyl-pyrimidine (1.7 g, 9.87 mmol) was dissolved in DMF:THF (3:1 24 mL). Tributylvinyltin (3.2 mL, 10.8 mmol) and Pd(PPh3)4 (0.148 g, 0.128 mmol) was added to this solution at RT under nitrogen and was heated at 120° C. for 30 min. The reaction mixture was cooled to RT and diluted with water (60 mL) and extracted with DCM (3×100 mL). The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure using rotary evaporator below 40° C. The crude was purified through column chromatography (20% Ethyl acetate-Hexane in silica 100-200 mesh, Diameter of column—5.0 cm, Height of silica—approx. 5 inch) to provide 2-methyl-5-vinylpyrimidine a as light yellow liquid (1.1 g, 91% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409910B2
Source datasetuspto-grants-2016_08
ORD IDord-56aa126835a34430936dfa51af7a8310
Source noteuspto-grants-2016_08