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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090399Generated: November 1, 2026

Potassium tert-butoxide → HCID 14770862, compound

https://huagongshe.com/reaction/1090399

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178471862HCID 178471862—
Solventtert-ButanolHCID 6386—
ProductHCID 14770862HCID 1477086286.2%

Reaction Steps

A solution of 21.4 g (50 mmol) of α-[(cyclopropylamino) methylene]-4-(1,4-dioxaspiro[4.4]non-7-yl)-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 150 ml of dry t-butanol. The resulting suspension was stirred at 65° for 4 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 17.3 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05081254
Source datasetuspto-grants-1992_01
ORD IDord-40e239f3a4a44f65b90c8da6eadacf73
Source noteuspto-grants-1992_01