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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 3-Benzo[b]thiophen-2-yl-1H-5-indazolecarbonitrile | HCID 22260732 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-Benzo[b]thiophen-2-yl-1H-5-indazolecarboxylic Acid | HCID 22260665 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07776890B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-bbd7f2500aab4d89826c9607d4fbeb8c |
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| Source note | uspto-grants-2010_08 |
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