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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2428192Generated: October 25, 2026

Ethyl Acetate → (3R,4S)-4-{4-[2-(2,6-Dichloro-4-methyl-phenoxy)-ethoxy]-phenyl}-piperidine-1,3-dicarboxylic Acid 1-tert-butyl Ester 3-methyl Ester

https://huagongshe.com/reaction/2428192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant4-{4-[2-(2,6-Dichloro-4-methylphenoxy)ethoxy]phenyl}piperidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-methyl esterHCID 67148722—
ReactantHCID 178418582HCID 178418582—
SolventMethanolHCID 887—
Product(3R,4S)-4-{4-[2-(2,6-Dichloro-4-methyl-phenoxy)-ethoxy]-phenyl}-piperidine-1,3-dicarboxylic Acid 1-tert-butyl Ester 3-methyl EsterHCID 6714835647.3%

Reaction Conditions

Temperature70 °C

Reaction Steps

MeONa (2.27 g, 42 mmol) was added to a sol. of compounds D5 (22.6 g, 42 mmol) in MeOH (200 mL). The mixture was stirred at 70° C. for 6 h, and MeONa (2.27 g, 42 mmol) was added again. The mixture was stirred at 70° C. for 2 days, and was allowed to cool to rt. EtOAc was added, and the resulting mixture was washed with aq. 1M HCl and brine. The org. layer was dried over MgSO4, filtered, and the solvents were removed under reduced pressure. Purification of the crude by FC (MeOH/CH2Cl2 5:95→10:90) yielded the title compound (10.7 g, 47%). LC-MS: tR=1.19 min, ES+=538.39.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968720B2
Source datasetuspto-grants-2011_06
ORD IDord-bd4d4809daea4306a7e37d0ee08b8df4
Source noteuspto-grants-2011_06