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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1854150Generated: October 31, 2026

Acetic Anhydride → methyl 6-(trifluoromethyl)-1H-indazole-4-carboxylate

https://huagongshe.com/reaction/1854150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTert-Butyl nitriteHCID 10906—
Reactant18-Crown-6HCID 28557—
ReactantPotassium AcetateHCID 517044—
ReactantMethyl 3-amino-2-methyl-5-(trifluoromethyl)benzoateHCID 68295733—
SolventChloroformHCID 6212—
Productmethyl 6-(trifluoromethyl)-1H-indazole-4-carboxylateHCID 6944114090%

Reaction Steps

To a stirred solution of methyl 3-amino-2-methyl-5-(trifluoromethyl)benzoate (1 equiv.) in chloroform (13 mL per 1 mmol), potassium acetate (1.05 equiv.) and acetic anhydride (2 equiv.) were added and reaction mixture stirred at room temperature for 12 h. After this time, tert-butyl nitrite (4 equiv.) and 18-crown-6 (0.35 equiv.) were added and reaction stirred again at 65° C. for 3 h. On completion, the reaction mixture was cooled to room temperature, diluted with chloroform (500 mL) and washed with sat. sodium bicarbonate solution. the organic layer was dried over sodium sulfate and concentrated to afford title the compound (yield 90-95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962620B2
Source datasetuspto-grants-2015_02
ORD IDord-e70f7cea4efd4071b0fe135bc43295b9
Source noteuspto-grants-2015_02