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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182336Generated: November 1, 2026

Methanol → methyl 1H-indazole-3-carboxylate

https://huagongshe.com/reaction/2182336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSulfuric AcidHCID 1118—
ReactantIndazole-3-carboxylic acidHCID 78250—
Productmethyl 1H-indazole-3-carboxylateHCID 657476—

Reaction Steps

0.5 ml of concentrated sulphuric acid (95%) is added dropwise, at a temperature in the region of 20° C., to a solution of 9.13 g of 3-indazolecarboxylic acid in 100 ml of methanol. After refluxing for 20 hours, the reaction medium is concentrated under reduced pressure at a temperature in the region of 40° C. The aqueous residue obtained is extracted with dichloromethane. The organic phases are combined, washed with water until neutral, dried over magnesium sulphate and then concentrated under reduced pressure at a temperature in the region of 40° C. The yellow powder obtained is washed with ethyl ether. A white powder is obtained. The filtrate is concentrated under reduced pressure until a yellow powder is obtained. This yellow powder is washed again with ethyl ether until a white powder is obtained. The yellow filtrate is concentrated a third time under reduced pressure and the yellow powder collected is itself also washed with ethyl ether. All the fractions of white powder are combined. 7.08 g of methyl 3-indazolecarboxylate are thus obtained in the form of a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897208B2
Source datasetuspto-grants-2005_05
ORD IDord-bdffaecf1cb94a81bbce24d845f93c4f
Source noteuspto-grants-2005_05