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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242584Generated: October 28, 2026

1-tert-Butyl 3-methyl 3-methyl-4-oxopiperidine-1,3-dicarboxylate → HCID 66758618, compound

https://huagongshe.com/reaction/242584

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-tert-Butyl 3-methyl 3-methyl-4-oxopiperidine-1,3-dicarboxylateHCID 66758517—
ReactantHCID 178478191HCID 178478191—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66758618HCID 6675861870.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

3-Methyl-4-oxo-piperidine-1,3-dicarboxylic acid-1-tert-butyl ester 3-methyl ester (1.1 g, 4.07 mmol) was dissolved in tetrahydrofuran and cooled to 0° C. To the solution was added 4-chlorophenyl magnesium bromide (12.2 mL, 12.2 mmol) dropwise over ˜½ h and then stirred at 0° C. for 1 h. The reaction was quenched with saturated solution of NH4Cl and extracted with ethyl acetate (3×). The organics were collected, dried over Mg2SO4, filtered and evaporated in vacuo, then purified by Biotage flash chromatography (10% ethyl acetate/90% hexane to 20% ethyl acetate/80% hexane) to yield the title compound (1.1 g, 70%). 1H-NMR (CDCl3): δ 1.17 (s, 3H), 1.44 (s, 9H), 1.55 (m, 1H), 1.96 (d, 1H) 3.00 (m, 1H), 3.37 (m, 2H), 3.53 (s, 3H), 3.91 (m, 2H), 4.07 (d, 1H), 7.27 (d, 2H), 7.43 (d, 2H). ESI-MS m/z: 384.1 (M+1), retention time 2.95.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653096B2
Source datasetuspto-grants-2014_02
ORD IDord-dc82fbe12f90417b8d3939e65e930558
Source noteuspto-grants-2014_02