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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15729Generated: October 25, 2026

Ammonium Hydroxide → Benzyl 2-(4-chlorophenyl)-4-oxopiperidine-1-carboxylate

https://huagongshe.com/reaction/15729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantAmmonium ChlorideHCID 25517—
ReactantBenzyl 3,4-dihydro-4-oxo-pyridine-1(2H)-carboxylateHCID 11368235—
ReactantHCID 178478191HCID 178478191—
ReactantHCID 178494437HCID 178494437—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductBenzyl 2-(4-chlorophenyl)-4-oxopiperidine-1-carboxylateHCID 59342393—

Reaction Conditions

Temperature-78 °C

Reaction Steps

CuBr.SMe2 complex (1.49 g, 7.26 mmol) was added to 25 mL of anhydrous THF and cooled to −78° C. 4-Chlorophenylmagnesium bromide (7.26 mL, 1.0 M in THF, 7.26 mmol) was added slowly via syringe. Stirring at −78° C. for 1 hour produced an orange then green-like suspension. Boron trifluoride dimethyl etherate (0.92 mL, 7.26 mmol) was added and stirred for 5 minutes. To the newly formed complex was then added over 1 hour a solution of the compound 66 (1.0 g, 4.32 mmol) in 15 mL of anhydrous THF. After stirring 2 hours at −78° C., 16 mL of aq. 20% NH4Cl/conc. NH4OH (1:1) was added, and the mixture was allowed to warm-up to room temperature. EtOAc was used to extract (3×100 mL) and the combined organic layers were washed with brine and dried (MgSO4). Solvent was removed by rotary evaporation and the residue was purified by flash chromatography to give the product 67 as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732609B2
Source datasetuspto-grants-2010_06
ORD IDord-ab71bfae619241b3a6352d150f024773
Source noteuspto-grants-2010_06