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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436123Generated: November 3, 2026

Ethyl Acetate → methyl(R)-2-tert-butoxycarbonylamino-6-(3,4-difluorophenyl)-6-oxohexanoate

https://huagongshe.com/reaction/1436123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-(Tert-butyl) 2-methyl (R)-6-oxopiperidine-1,2-dicarboxylateHCID 10729829—
ReactantHCID 178505835HCID 178505835—
SolventTetrahydrofuranHCID 8028—
Productmethyl(R)-2-tert-butoxycarbonylamino-6-(3,4-difluorophenyl)-6-oxohexanoateHCID 67461441—

Reaction Conditions

Temperature-40 °C

Reaction Steps

To a solution of (R)-6-oxopiperidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester (CAS No. 183890-36-0, 5.8 g) in THF (200 mL), 3,4-difluorophenylmagnesium bromide (0.5 M solution in THF, 50 mL) was added dropwise at −40° C., and the reaction solution was stirred at −40° C. for seven hours. A saturated ammonium chloride solution and ethyl acetate were added to the reaction solution, and the mixture was heated to room temperature. Thereafter, the organic layer was separated, and the resulting organic layer was dried over magnesium sulfate and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (elution solvent: heptane->heptane:ethyl acetate=1:1) to obtain 3.8 g of the title compound. The property value of the compound is as follows.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618960B2
Source datasetuspto-grants-2009_11
ORD IDord-b3d3a3412d374834a217a560784c503b
Source noteuspto-grants-2009_11