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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750724Generated: November 3, 2026

Ethyl 4-(4-oxopiperidin-1-yl)benzoate → Ethyl 4-(4-(cyclohexylmethyl)-4-hydroxypiperidin-1-yl)benzoate

https://huagongshe.com/reaction/1750724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-(4-oxopiperidin-1-yl)benzoateHCID 12717442—
ReactantHCID 178419664HCID 178419664—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-(4-(cyclohexylmethyl)-4-hydroxypiperidin-1-yl)benzoateHCID 16109048—

Reaction Steps

A solution of cyclohexylmethylmagnesium bromide (1.90 mL of a 2M solution in THF) at −78° C. was treated with ethyl 4-(4-oxo-1-piperidinyl)benzoate (prepared according to the procedure described in Synthesis 1981, 606-608, 0.30 g), and was allowed to warm to room temperature overnight. The reaction mixture was partitioned between ethyl acetate and saturated aqueous NH4Cl and the aqueous layer was extracted with ethyl acetate (2×). The combined organic layers were dried (MgSO4), filtered, and concentrated. The resulting residue was purified by silica gel chromatography eluting with 20% ethyl acetate to give the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156856B2
Source datasetuspto-grants-2015_10
ORD IDord-26800ac6c0ed45c99a8ffc1746fb3bfe
Source noteuspto-grants-2015_10