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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651591Generated: November 2, 2026

Potassium tert-butoxide → HCID 14770861, compound

https://huagongshe.com/reaction/1651591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178471863HCID 178471863—
Solventtert-ButanolHCID 6386—
ProductHCID 14770861HCID 1477086182.4%

Reaction Steps

A solution of 21.0 g (50 mmol) of 4-[3-(acetylamino) cyclopentyl]-α-[(cyclopropylamino)methylene]-2,5-difluoro-β-oxobenzenepropanoic acid, ethyl ester in 250 ml of dry t-butanol was treated with a slurry of 6.2 g (55 mmol) of potassium t-butoxide in 50 ml of dry t-butanol. The resulting suspension was stirred and heated at 65° for 3 hours and then at room temperature overnight. The solvent was removed in vacuo and the residue was dissolved in methylene chloride and washed with 1.0 M hydrochloric acid. After drying (MgSO4) and evaporating the solvent in vacuo, the residue was recrystallized from ethyl acetate/hexane to give 16.5 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04929613
Source datasetuspto-grants-1990_05
ORD IDord-25d5d4407c244eceabaad447da9f40e1
Source noteuspto-grants-1990_05