HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589286Generated: October 30, 2026
Water → 7-(Trifluoromethyl)-1-benzothiophene-2-carboxylic acid
https://huagongshe.com/reaction/589286
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | Methyl 7-(trifluoromethyl)-1-benzothiophene-2-carboxylate | HCID 18526203 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 7-(Trifluoromethyl)-1-benzothiophene-2-carboxylic acid | HCID 17979623 | 83.5% |
Reaction Steps
A mixture of 800 mg of methyl 7-(trifluoromethyl)benzo[b]thiophene-2-carboxylate, 154 mg of lithium hydroxide monohydrate, 4 ml of water and 12 ml of methanol was stirred at 75° C. for 2 hours. The reaction mixture was cooled to room temperature, and then concentrated under reduced pressure. To the residue was added water, and then washed with tert-butyl methyl ether 3 times. To the aqueous layer was added concentrated hydrochloric acid, and then extracted with tert-butyl methyl ether 3 times. The combined organic layer was washed with saturated aqueous sodium chloride solution, dried over magnesium sulfate, and then concentrated under reduced pressure to obtain 632 mg of 7-(trifluoromethyl)benzo[b]thiophene-2-carboxylic acid (the present compound 4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09232792B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-64ea382c66a94c9d837d6c641bcc757d |
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| Source note | uspto-grants-2016_01 |
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