HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388644Generated: October 29, 2026
Potassium tert-butoxide → HCID 178487696, compound
https://huagongshe.com/reaction/388644
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 4-trifluoromethyl-4H-thiazole-2-carboxylic acid-(6-acetyl-3-methoxy-2-methyl-phenyl)-amide | HCID 66730375 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 178487696 | HCID 178487696 | 89% |
Reaction Steps
To a solution of compound 202b (70 g, 1 eq.) in tBuOH (1.2 L) was added potassium t-butoxide (46 g, 2.1 eq.) under nitrogen. The mixture was heated to 70° C. for 16 hrs. The reaction mixture was concentrated under reduced pressure and then acidified to pH 5. The precipitate was filtered, washed with water, and triturated in a diisopropylether/pentane mixture to yield compound 203b as a beige solid in 89% yield. 1H NMR (CDCl3, 400 MHz) δ (ppm) 2.43 (s, 3H), 3.98 (s, 3H), 6.76 (d, J=1.76 Hz, 1H), 7.04 (d, J=9.10 Hz, 1H), 7.96 (s, 1H), 8.24 (d, J=9.10 Hz, 1H), 9.31 (brs, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08377962B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-512532bde4f648b094ff1e24a281b7b9 |
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| Source note | uspto-grants-2013_02 |
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