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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522503Generated: October 28, 2026

2-Furancarbonyl chloride → HCID 58526528, compound

https://huagongshe.com/reaction/522503

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Furancarbonyl chlorideHCID 68242—
Reactant4,6-DichloropyrimidineHCID 70943—
ReactantLithium ChlorideHCID 433294—
ReactantHCID 178418546HCID 178418546—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58526528HCID 5852652871%

Reaction Conditions

Temperature25 °C

Reaction Steps

4,6-Dichloropyrimidine 6 (149 mg, 1.0 mmol) in THF (2 mL) was added to a solution of TMPZnCl.LiCl (2) (1.3 M in THF, 0.85 mL, 1.1 mmol) at 25° C. and the reaction mixture was then stirred at this temperature for 45 min according to TP 2. CuCN.2LiCl (1.0 M solution in THF, 1.1 mL, 1.1 mmol) was slowly added at −20° C. and the reaction mixture was stirred at the same temperature for 30 min. Then, furan-2-carbonyl chloride (261 mg, 2.0 mmol) was dropwise added at −20° C. and the resulting mixture was allowed to warm up slowly to 25° C. overnight. The reaction mixture was quenched with a sat. aq. NH4Cl solution (30 mL), extracted with diethyl ether (5×30 mL) and dried over anhydrous Na2SO4. After filtration, the solvent was evaporated in vacuo. Purification by flash-chromatography (CH2Cl2/n-pentane 1:1) furnished 8b as a colourless solid (172 mg, 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334237B2
Source datasetuspto-grants-2016_05
ORD IDord-4d488838323f4555a4e464aa7d882f50
Source noteuspto-grants-2016_05