HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925730Generated: October 27, 2026
Lithium Hydroxide → 3-[2-Bromo-4-(trifluoromethyl)phenylsulfonamido]thiophene-2-carboxylic acid
https://huagongshe.com/reaction/1925730
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Methyl 3-[2-bromo-4-(trifluoromethyl)phenylsulfonamido]thiophene-2-carboxylate | HCID 67520727 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-[2-Bromo-4-(trifluoromethyl)phenylsulfonamido]thiophene-2-carboxylic acid | HCID 25183650 | 34.6% |
Reaction Steps
To a solution of 97 (330.0 mg; 0.74 mmol) in tetrahydrofuran (8 mL) and methanol (2 mL) was added aqueous lithium hydroxide (4 mL; 2M). The reaction mixture was heated at 75-80° C. for 6 hours, allowed to cool to room temperature and then concentrated under reduced pressure. The resulting residue was dissolved in chloroform (15 mL) and washed with aqueous hydrochloric acid (2×10 mL; 2N). The organic phase was dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The crude residue was purified by preparative HPLC to afford the title compound as a white solid (110 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08178699B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-55868052b5554a7fbc3f726d4708967e |
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| Source note | uspto-grants-2012_05 |
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