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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203152Generated: October 30, 2026

Acetic Anhydride → Methyl 5-(trifluoromethyl)-1H-indazole-7-carboxylate

https://huagongshe.com/reaction/2203152

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantIsoamyl NitriteHCID 8053—
ReactantPotassium AcetateHCID 517044—
ReactantMethyl 2-amino-3-methyl-5-(trifluoromethyl)benzoateHCID 118251663—
SolventChloroformHCID 6212—
ProductMethyl 5-(trifluoromethyl)-1H-indazole-7-carboxylateHCID 118251578—

Reaction Steps

To a solution of compound 3, at 0° C. and under nitrogen atmosphere, in chloroform (0.3M) was added acetic anhydride (2.3 equiv.) drop wise and the resulting mixture was stirred for 1 h at r.t. Then potassium acetate (0.2 equiv.) was added followed by addition of isoamyl nitrite (2.2 equiv.) and the resulting mixture was heated at reflux for 16 h. After, the reaction was cooled down to r.t. While cooling, a solid precipitation was observed. The solid was filtrated and dried under vacuum to give the title compound 4. (0.324 g, 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365569B2
Source datasetuspto-grants-2016_06
ORD IDord-d6c86550ca0542cba895e693e06802bb
Source noteuspto-grants-2016_06