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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651589Generated: November 2, 2026

Potassium tert-butoxide → HCID 14770859, compound

https://huagongshe.com/reaction/1651589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178471864HCID 178471864—
Solventtert-ButanolHCID 6386—
ProductHCID 14770859HCID 14770859—

Reaction Conditions

Temperature65 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04929613
Source datasetuspto-grants-1990_05
ORD IDord-7d99f05236294f12a30ee346cb508eb6
Source noteuspto-grants-1990_05