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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2360976Generated: October 30, 2026

Ethyl Acetate → HCID 67384774, compound

https://huagongshe.com/reaction/2360976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantMethyl 4-(bromomethyl)benzoateHCID 256687—
ReactantLithium diisopropylamideHCID 2724682—
Reactant4-Benzyl 1-tert-butyl piperidine-1,4-dicarboxylateHCID 22255913—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67384774HCID 67384774—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of piperidine-1,4-dicarboxylic acid 4-benzyl ester 1-tert-butyl ester (30.12 mmol; 9.62 g) in dry THF (100 mL) under argon at −78° C. was added, dropwise, a 2M solution of lithium diisopropylamide (2M solution in heptanes/THF/ethylbenzene; 39.16 mmol; 19.58 mL). The resulting solution was stirred at −78° C. for 2 hours. 4-Bromomethylbenzoic acid methyl ester (30.12 mmol; 6.90 g) was added and the resulting solution was stirred at −78° C. for 2 hours and allowed to warm to room temperature overnight. Ethyl acetate (150 ml) was added. The resulting solution was washed with a 1M aqueous hydrochloric acid solution (2×50 mL) and brine (50 mL) and dried over magnesium sulfate. After filtration and evaporation, the residue was purified via flash column chromatography (eluent gradient: 0 to 50% EtOAc in heptane) to yield 4-(4-methoxycarbonyl-benzyl)-piperidine-1,4-dicarboxylic acid 4-benzyl ester 1-tert-butyl ester. MS (ESI) m/z 468.20 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08686152B2
Source datasetuspto-grants-2014_04
ORD IDord-efc6c75beba94dbbac807b126aef372d
Source noteuspto-grants-2014_04