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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-Chloro-2-iodopyrimidine | HCID 29938005 | — |
| Reactant | HCID 178471816 | HCID 178471816 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | Ethyl 3-(5-chloropyrimidin-2-yl)propanoate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09416111B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-3ace5a00046a46a28ff19890d33d5de1 |
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| Source note | uspto-grants-2016_08 |
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