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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369617Generated: November 1, 2026

4-Chlorophenol → Methyl 4-(4-chlorophenoxy)thieno[2,3-c]pyridine-2-carboxylate

https://huagongshe.com/reaction/1369617

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorophenolHCID 4684—
ReactantCesium carbonateHCID 10796—
Reactant3,5-Dichloro-4-pyridinecarboxaldehydeHCID 2762988—
Reactant2-MercaptopropionateHCID 15607736—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-(4-chlorophenoxy)thieno[2,3-c]pyridine-2-carboxylateHCID 10892544—

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 4-chlorophenol (2.63 g, 20.5 mmol) in THF (20 mL) at 0° C. was treated dropwise with a solution of potassium tert-butoxide (1.0 M solution in THF, 20.4 mL, 20.5 mmol), stirred at 25° C. for 1 hour, cooled to 0° C., treated with a solution of Example 17A (3.54 g, 20.23 mmol) in THF (40 mL), warmed at 60° C. for 0.5 hours, cooled to 0° C., treated with methylthioglycolate (1.989 mL, 22.25 mmol) and Cs2CO3 (6.59 g, 20.23 mmol), warmed at 60° C. for 0.25 hours, cooled to room temperature and filtered. The filtrate was diluted with ethyl acetate, washed sequentially with water and brine, dried (MgSO4), filtered, and concentrated. Purification of the residue by flash chromatography on silica gel with 4% acetone/hexane provided the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06579882B2
Source datasetuspto-grants-2003_06
ORD IDord-b19741223c0e4dddb9e0be38212474aa
Source noteuspto-grants-2003_06