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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1870478Generated: October 30, 2026

N,N-Diethylaniline → HCID 22992851, compound

https://huagongshe.com/reaction/1870478

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DiethylanilineHCID 7061—
ReactantPotassium CarbonateHCID 11430—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant1-Bromo-4-chlorobutaneHCID 81364—
ReactantHCID 22992846HCID 22992846—
SolventAcetoneHCID 180—
ProductHCID 22992851HCID 2299285143%

Reaction Conditions

Temperature90 °C

Reaction Steps

918 mg of 8-chloro-2,3,4,5-tetrahydro-1,4-benzoxazepine-3,5-dione was dissolved in 20 ml of acetone, 1.2 g (2 equivalents) of potassium carbonate and 819 mg (1.1 equivalents) of 1-bromo-4-chlorobutane were added, and the mixture heated and refluxed for 7 hours. The resultant mixture was allowed to cool, then filtered. The filtrate was condensed and the residue obtained was dissolved in 2 ml of phosphorus oxychloride. Further, 1.4 ml (2 equivalents) of N,N-diethylaniline was added and the mixture was stirred at 90° C. for 12 hours. The phosphorus oxychloride was distilled off and a 10% sodium hydroxide aqueous solution added under ice cooling. The mixture was extracted with methylene chloride, then was washed with a saturated aqueous solution of potassium bicarbonate and saturated saline and dried over anhydrous magnesium sulfate. The solvent was distilled off and the crude product obtained was purified by silica gel column chromatograph (hexane:ethyl acetate=6:1) to obtain 598 mg of the above-identified compound (yield 43%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06096884
Source datasetuspto-grants-2000_08
ORD IDord-f00cb79a1e9c499692004f162fc11203
Source noteuspto-grants-2000_08