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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2042989Generated: October 30, 2026

2-Chloro-4-iodopyridine → Methyl 4-[2-(2-chloro-4-pyridinyl)ethynyl]benzenepropanoate

https://huagongshe.com/reaction/2042989

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-4-iodopyridineHCID 1516511—
ReactantMethyl 3-(4-Ethynylphenyl)propanoateHCID 25150216—
ProductMethyl 4-[2-(2-chloro-4-pyridinyl)ethynyl]benzenepropanoateHCID 54757928—

Reaction Steps

The title compound was prepared from methyl 3-(4-ethynylphenyl)propanoate (104 mg, 0.55 mmol) and 2-chloro-4-iodopyridine (141 mg, 0.59 mmol) according to the general procedure IC to give 96 mg (58%) of a pale yellow solid after purification by flash chromatography (SiO2, EtOAc/hexanes, 1:5). Rf: 0.22 (EtOAc:hexanes, 1:5); 1HNMR (CDCl3) δ 8.36-8.35 (m, 1H), 7.48-7.45 (m, 2H), 7.42-7.41 (m, 1H), 7.29-7.26 (m, 1H), 7.24-7.21 (m, 2H), 3.67 (s, 3H), 3.01-2.96 (t, 2H, J=7.8 Hz), 2.67-2.62 (t, 2H, J=7.8 Hz); 13CNMR (CDCl3) δ 172.9, 151.7, 149.5, 142.4, 134.4, 132.1, 128.6, 125.9, 124.1, 95.4, 85.3, 51.8, 35.2, 30.8; EI-MS calcd for C17H15ClNO2 (M+): 299. found: 299.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586607B2
Source datasetuspto-grants-2013_11
ORD IDord-2190f3ef2537416380742be2aefda2fa
Source noteuspto-grants-2013_11