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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042317Generated: November 1, 2026

Potassium tert-butoxide → HCID 58133378, compound

https://huagongshe.com/reaction/1042317

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 58133380HCID 58133380—
SolventDimethylformamideHCID 6228—
ProductHCID 58133378HCID 58133378—

Reaction Steps

To a solution of 2-{[2-(2,6-diethyl-4-methyl-phenyl)-acetyl]-methyl-amino}-nicotinic acid methyl ester (300 mg) in N,N-dimethylformamide (5 ml) was added potassium tert-butoxide (250 mg). The reaction mixture was stirred at ambient temperature for 18 hours, and then at 50° C. for 2 hours. The reaction mixture was partitioned the reaction between water and dichloromethane. The phases were separated and the aqueous phase was extracted with further dichloromethane and ethyl acetate. The aqueous phase was acidified by addition of aqueous hydrochloric acid (2M) and extracted three times with ethyl acetate. The combined organic extracts were dried over magnesium sulfate and concentrated. The residue was passed through a plug of silica eluting with ethyl acetate to give Compound No. D20 of Table D as an off-white solid (320 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557840B2
Source datasetuspto-grants-2013_10
ORD IDord-3522a1d9ae62482d8229d41c69af4b0b
Source noteuspto-grants-2013_10