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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1480040Generated: October 26, 2026

Hydrochloric Acid → 5-Chloro-4-cyclopropylmethoxy-pyridine-2-carboxylic acid

https://huagongshe.com/reaction/1480040

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantCyclopropanemethanolHCID 75644—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant5-Chloro-4-iodo-2-pyridinecarboxylic acidHCID 85592091—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product5-Chloro-4-cyclopropylmethoxy-pyridine-2-carboxylic acidHCID 9020363857.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 5-chloro-4-iodo-pyridine-2-carboxylic acid (CAN 120643-06-3, 600 mg, 2.12 mmol) in THF (20 mL) and DMF (2 mL) was added with stirring potassium tert-butoxide (1.0 g, 8.91 mmol) and cyclopropanemethanol (1.5 mL, 18.8 mmol). The resulting mixture was stirred at 80° C. for 25 h, cooled, acidified with hydrochloric acid (25 mL, 1 N) and partitioned into ethyl acetate. The organic portions were combined, dried over Na2SO4, filtered and concentrated. The residue was purified by prep. HPLC (Gemini NX, acetonitrile/water gradient) to give the title compound (276 mg, 57%) as light yellow solid. MS (ESI, m/z): 228.4 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409866B2
Source datasetuspto-grants-2016_08
ORD IDord-facf010612ba417b850001705fe85ca0
Source noteuspto-grants-2016_08