HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 925930Generated: October 30, 2026
Potassium tert-butoxide → HCID 178437374, compound
https://huagongshe.com/reaction/925930
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 4-Trimethylsilanylethynyl-thiazole-2-carboxylic acid-(6-acetyl-3-methoxy-2-methyl-phenyl)-amide | HCID 67214021 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 178437374 | HCID 178437374 | 52% |
Reaction Steps
To a suspension of compound 208b (8.71 g, 1 eq.) in tert-butanol (240 mL) was added potassium tert-butoxide (5.32 g, 2.1 eq.). The heterogeneous mixture was stirred and heated to 80° C. The solvent was then evaporated and water was added to the resulting black residue. The pH of the mixture was brought to 6 with 1N HCl. The mixture was extracted with dichloromethane. The organic layer was dried over Na2SO4, filtered, and concentrated under vacuo. The solid was purified by chromatography on silica gel to give compound 209b as an orange solid in 52% yield. 1H NMR (CDCl3, 400 MHz) δ (ppm) 2.45 (s, 3H), 3.25 (s, 1H), 3.99 (s, 3H), 6.89 (br s, 1H), 7.06 (d, J=9.09 Hz, 1H), 7.72 (s, 1H), 8.26 (d, J=9.09 Hz, 1H), 9.50 (br s, 1H); MS (ESI, EI+): m/z=297 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09284307B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-ed1742d2fbae426f99103fe32eb661ac |
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| Source note | uspto-grants-2016_03 |
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