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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728315Generated: November 1, 2026

Ammonium Chloride → Methyl 2-oxo-5-(pyridin-4-yl)cyclohexane-1-carboxylate

https://huagongshe.com/reaction/728315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 53880921HCID 53880921—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-oxo-5-(pyridin-4-yl)cyclohexane-1-carboxylateHCID 1398605339.8%

Reaction Steps

To 100 ml of tetrahydrofuran, there was added 13 g of potassium t-butoxide. A solution of 26 g of 4-(4-pyridyl)pimelic acid methyl ester in 50 ml of tetrahydrofuran was added at 20° to 40° C. and the mixture was stirred for 2 hours. After the reaction was completed, the mixture was treated with saturated aqueous solution of ammonium chloride and then extracted with ether. The ether solution was washed with water and dried. Ether was distilled off and the residue was recrystallized from ether. There was obtained 9.6 g of 2-methoxycarbonyl-4-(4-pyridyl)cyclohexanone: m.p. 82°-83° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05047545
Source datasetuspto-grants-1991_09
ORD IDord-544212aabfe7409a911fa91d30ca9b96
Source noteuspto-grants-1991_09