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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2054452Generated: November 2, 2026

N,N-Dimethylaniline → HCID 59134773, compound

https://huagongshe.com/reaction/2054452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
Reactanttert-Butyl 4-(Chlorocarbonyl)piperidine-1-carboxylateHCID 21906247—
ReactantHCID 59655945HCID 59655945—
SolventDichloromethaneHCID 6344—
ProductHCID 59134773HCID 59134773—

Reaction Steps

N,N-dimethylaniline (7.12 mL, 56.2 mmol) followed by tert-butyl 4-(chlorocarbonyl)piperidine-1-carboxylate 1-11 (42.1 mL of a 1 M solution in methylene chloride, 42.1 mmol) were added to a neat stirred mixture of 2-bromo-N-isopropyl-4,5-dimethylaniline 1-9 (6.80 g, 28.1 mmol) and N,N-dimethylamino-pyridine (172 mg, 1.40 mmol) at approximately 0° C. The resulting mixture was heated to reflux for 30 min, cooled to ambient temperature and partitioned between diethyl ether and aqueous 1 N hydrochloric acid. The organic phase was separated and washed successively with aqueous 1 N hydrochloric acid, saturated aqueous sodium bicarbonate, brine, dried (sodium sulfate) and concentrated in vacuo to give a crude residue. Purification of the crude residue by flash chromatography over silica gel (gradient elution; 0%-40% ethyl acetate/hexanes as eluent) afforded 1-12 as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07329673B2
Source datasetuspto-grants-2008_02
ORD IDord-d82c6b69706646098d67d1c1f0e53e7f
Source noteuspto-grants-2008_02