HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651589Generated: November 2, 2026
Potassium tert-butoxide → HCID 14770859, compound
https://huagongshe.com/reaction/1651589
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 178471864 | HCID 178471864 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 14770859 | HCID 14770859 | — |
Reaction Steps
A solution of 3.91 g (10 mmoles) of ethyl α-[(cyclopropylamino)methylene]-2,5-difluoro-4-(1-methyl-4-piperidinyl)-β-oxobenzenepropanoate in 50 ml of t-butyl alcohol was treated with 1.23 g (11 mmoles) of potassium t-butoxide and heated at 65° C. for 11/2 hours. The mixture was evaporated under vacuum and the residue was stirred in 50 ml of water and neutralized with 1 N HCl. After extraction with chloroform the organic layer was dried (MgSO4) and evaporated to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04929613 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-7d99f05236294f12a30ee346cb508eb6 |
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| Source note | uspto-grants-1990_05 |
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