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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090403Generated: October 30, 2026

Potassium tert-butoxide → HCID 14770828, compound

https://huagongshe.com/reaction/1090403

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178471866HCID 178471866—
Solventtert-ButanolHCID 6386—
ProductHCID 14770828HCID 14770828—

Reaction Steps

A solution of 3.49 g (8.30 mmol) ethyl 4-(1-acetyl-4-piperidinyl)-α-[(cyclopropylamino)methylene]-2,5-difluoro-β-oxobenzenepropionate in 35 ml of t-butyl alcohol was treated with 0.93 g (8.30 mmol) potassium t-butoxide and stirred in an oil bath at 65° for 1.5 hours. The mixture was evaporated under vacuum and the residue extracted with 0.5 N hydrochloric acid. The organic layer was dried (MgSO4) and evaporated. The title compound was isolated by chromatography on silica gel and crystallization from toluene, mp 195°-201° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05081254
Source datasetuspto-grants-1992_01
ORD IDord-bce2c3cc066f4cd18d969d3fe43daa80
Source noteuspto-grants-1992_01