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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639735Generated: October 30, 2026

Potassium Acetate → methyl 1H-indazole-4-carboxylate

https://huagongshe.com/reaction/1639735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium AcetateHCID 517044—
ReactantBenzoic acid, 2-amino-6-methyl-, methyl esterHCID 583916—
ReactantAmmonium fluoroborateHCID 9964072—
ReactantSodium NitriteHCID 23668193—
CatalystHydrochloric AcidHCID 313—
Catalyst18-Crown-6HCID 28557—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
Productmethyl 1H-indazole-4-carboxylateHCID 662332759.1%

Reaction Steps

A mixture of methyl 3-amino-o-toluate (100 g, 605 mmol), a solution of ammonium tetrafluoroborate (83.0 g, 787 mmol) in water (600 mL) and concentrated hydrochloric acid (121 mL, 3.93 mmol) was cooled to 0° C., and a solution of sodium nitrite (41.8 g, 605 mmol) in water (88 mL) was added dropwise to the mixture over 25 min. This mixture was stirred for 35 min, and the resulting solid was collected by filtration. This solid was washed with water, methanol and diethyl ether, dried under nitrogen atmosphere, and added to a solution of potassium acetate (65.4 g, 666 mmol) and 18-crown-6 (4.50 g, 17.0 mmol) in chloroform (1.37 L). The resulting mixture was stirred at room temperature for 2 hr, and water (700 mL) was added. The partitioned organic layer was washed with water, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was triturated with hexane, and collected by filtration to give the title compound (63.0 g, yield 59%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110585B2
Source datasetuspto-grants-2012_02
ORD IDord-d3dc41a2ca944671967f0a15fb479d82
Source noteuspto-grants-2012_02