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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963702Generated: October 29, 2026

Acetic Acid → Ethyl 1-isopropylpiperidine-4-carboxylate

https://huagongshe.com/reaction/1963702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAcetoneHCID 180—
ReactantEthyl 4-piperidinecarboxylateHCID 70770—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
ProductEthyl 1-isopropylpiperidine-4-carboxylateHCID 19900430—

Reaction Steps

To ethylpiperidine-4-carboxylate (1 eq) in methanol was added acetone (1 eq) and acetic acid (5%) and the resulting mixture was stirred for 2 h at ambient temperature. To it was then added sodium cyanoborohydride (1 eq) and continued stirring for 16 h. The mixture was then concentrated and to it was added sodium bicarbonate and was partitioned between ethyl acetate and water. The organic layer was dried with sodium sulfate and concentrated to yield ethyl-1-(methylethyl)piperidine 4-carboxylate. To this was then added concentrated hydrochloric acid and water (2:1) and the mixture was refluxed for 5 h. The resulting 1-(methylethyl)piperidine-4-carboxylic acid was then azeotroped with toluene. MS: MH+=172.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415382B2
Source datasetuspto-grants-2013_04
ORD IDord-bb54a7b705c44f6fade2080d09478663
Source noteuspto-grants-2013_04