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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432623Generated: October 26, 2026

Tetrahydrofuran → 2-(4-Chloro-thiophen-2-yl)-6-methyl-pyridine

https://huagongshe.com/reaction/1432623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant2-Bromo-4-chlorothiopheneHCID 13780838—
ReactantHCID 178426002HCID 178426002—
CatalystHCID 178418397HCID 178418397—
SolventDiethyl EtherHCID 3283—
Product2-(4-Chloro-thiophen-2-yl)-6-methyl-pyridineHCID 6884008828%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of 2-bromo-4-chloro-thiophene (Gronowitz, Rosén Chemica Scripta, 1971, 1, 33) (1.50 g, 7.60 mmol) and 0.5 M solution of 6-methyl-2-pyridylzinc bromide in THF (23.00 mL, 11.39 mmol) is added Pd(PPh3)4 (0.18 g, 0.15 mmol). The solution is heated at 40° C. overnight, diluted with Et2O (50 mL), washed with sat. NH4Cl (40 mL), dried over MgSO4, filtered on concentrated. The residue is purified by ISCO column chromatography (5%-20% EtOAc/hexane gradient) furnish the title compound (0.45 g, 2.15 mmol, 28%). 1H NMR (CDCl3), δ 2.56 (s, 3H), 7.02 (d, 7.7 Hz, 1H), 7.13 (d, J=0.9 Hz, 1H), 7.36 (d, J=7.9 Hz, 1H), 7.39 (d, J=0.9 Hz, 1H), 7.54 (dd, J=7.9, 7.7, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612067B2
Source datasetuspto-grants-2009_11
ORD IDord-c389d7d85a6549479abb62a3329f701c
Source noteuspto-grants-2009_11