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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642465Generated: November 1, 2026

Tetrahydrofuran toluene → Ethyl 4-(4-hydroxy-1-piperidyl)-4-methyl-piperidine-1-carboxylate

https://huagongshe.com/reaction/1642465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuran tolueneHCID 22635083—
ReactantEthyl 4-cyano-4-(4-hydroxy-1-piperidyl)piperidine-1-carboxylateHCID 57619806—
ReactantHCID 178418689HCID 178418689—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-(4-hydroxy-1-piperidyl)-4-methyl-piperidine-1-carboxylateHCID 5761981865.5%

Reaction Steps

To a stirred solution of ethyl 4-cyano-4-(4-hydroxy-1-piperidyl)piperidine-1-carboxylate (2.45 g, 8.69 mmol) in THF (20 mL) was added a 1.4 M solution of MeMgBr in toluene/THF (18.6 mL, 26.1 mmol) at 0° C., and the mixture was stirred at room temperature for 12 h. The reaction was then quenched with saturated aqueous ammonium chloride, and the mixture was extracted with dichloromethane (2×25 mL). The combined extracts were concentrated in vacuo to afford the title compound (1.54 g, 65%), which was used in the next step without further purification. MS (M+1): 271.26.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119661B2
Source datasetuspto-grants-2012_02
ORD IDord-d6f4eb0725dd49f28bcc43cf5affb39a
Source noteuspto-grants-2012_02