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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1482877Generated: October 30, 2026

5-Chloro-2-iodopyrimidine → Ethyl 3-(5-chloropyrimidin-2-yl)propanoate

https://huagongshe.com/reaction/1482877

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-2-iodopyrimidineHCID 29938005—
ReactantHCID 178471816HCID 178471816—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventAmmonium ChlorideHCID 25517—
ProductEthyl 3-(5-chloropyrimidin-2-yl)propanoateHCID 118155027—

Reaction Steps

5-Chloro-2-iodopyrimidine (4 g, 16.64 mmol) and tetrakis(triphenylphosphine)palladium(0) (1.92 g, 1.66 mmol) were suspended in THF (83 mL). 3-Ethoxy-3-oxopropylzinc bromide (33.3 mL, 16.64 mmol) was added, and the resultant mixture was stirred at room temperature for 18 hours. The mixture was diluted with saturated ammonium chloride and water (1:1) and extracted with EtOAc (3×100 mL). The combined organic layers were washed with brine, dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo. The residue was purified by column chromatography on silica gel (EtOAc:Hexanes) to give ethyl 3-(5-chloropyrimidin-2-yl)propanoate. MS ESI calcd for C9H12ClN2O2[M+H]+ 215. found 215. 1H NMR (500 MHz, DMSO-d6) δ 8.82 (s, 2H), 4.00 (q, J=7.1 Hz, 2H), 3.13 (t, J=6.9 Hz, 2H), 2.78 (t, J=6.9 Hz, 2H), 1.11 (t, J=7.1 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09416111B2
Source datasetuspto-grants-2016_08
ORD IDord-3ace5a00046a46a28ff19890d33d5de1
Source noteuspto-grants-2016_08