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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503114Generated: October 30, 2026

Acetic Acid → 3-Benzo[b]thiophen-2-yl-1H-5-indazolecarboxylic Acid

https://huagongshe.com/reaction/503114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
ReactantSulfuric AcidHCID 1118—
Reactant3-Benzo[b]thiophen-2-yl-1H-5-indazolecarbonitrileHCID 22260732—
SolventEthyl AcetateHCID 8857—
Product3-Benzo[b]thiophen-2-yl-1H-5-indazolecarboxylic AcidHCID 22260665—

Reaction Conditions

Temperature110 °C

Reaction Steps

To 288 mg of 3-benzo[b]thiophen-2-yl-1H-5-indazolecarbonitrile were added 3 ml of glacial acetic acid, 1 ml of water and 0.8 ml of concentrated sulfuric acid, and the mixture was stirred at 110° C. for 4 hours. After standing to cool, the mixture was added with 120 ml of ethyl acetate, sequentially washed with water and brine, dried over anhydrous magnesium sulfate. After filtering the organic layer through a silica gel pat, the solvent was evaporated, to give 307 mg of the title compound as ocher yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776890B2
Source datasetuspto-grants-2010_08
ORD IDord-bbd7f2500aab4d89826c9607d4fbeb8c
Source noteuspto-grants-2010_08