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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1046096Generated: October 31, 2026

Potassium Fluoride → 2-Chloro-5-(1-ethoxyvinyl)pyrimidine

https://huagongshe.com/reaction/1046096

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium FluorideHCID 522689—
Reactant5-Bromo-2-chloropyrimidineHCID 606665—
ReactantStannane, tributyl(1-ethoxyethenyl)-HCID 619414—
CatalystHCID 178418476HCID 178418476—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product2-Chloro-5-(1-ethoxyvinyl)pyrimidineHCID 1432100261%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 5-bromo-2-chloropyrimidine (600 mg, 3.13 mmol) in dry DMF (10 mL) under N2 were added tributyl(1-ethoxyvinyl)stannane (1.09 mL, 3.23 mmol) and Pd(PPh3)2Cl2 (113 mg, 0.161 mmol). The mixture was stirred at 100° C. for 3 h and at rt for 16 h. The mixture was diluted with ether (20 mL), and treated with aqueous KF solution (5 g of KF in 3 mL of water). The mixture was stirred vigorously for 1 h at room temperature before being filtered through diatomaceous earth. The filtrate was washed with satd aq NaHCO3 and brine. The aqueous phase was extracted with EtOAc. The combined organic layer was dried over anhydrous Na2SO4 and concentrated to give 2-chloro-5-(1-ethoxyvinyl)pyrimidine (350 mg, yield 61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569292B2
Source datasetuspto-grants-2013_10
ORD IDord-9f770e1a805d415e9f445a0480a3d4a4
Source noteuspto-grants-2013_10