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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721606Generated: November 1, 2026

N,N-Dimethylaniline → HCID 15225152, compound

https://huagongshe.com/reaction/1721606

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
ReactantPyridineHCID 1049—
ReactantPiperidineHCID 8082—
ReactantDiphosgeneHCID 10426—
Reactant4-PhenoxyphenolHCID 13254—
SolventBenzeneHCID 241—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 15225152HCID 15225152182.3%

Reaction Steps

A solution of 4-phenoxyphenol (5.0 g, 26.9 mmol) and dimethylaniline (3.4 ml, 26.8 mmol) in 35 ml of benzene plus 1.5 ml of dioxane was added dropwise over 15 minutes under a nitrogen atmosphere to a solution of trichloromethyl chloroformate (1.6 ml, 13.3 mmol) in 30 ml of benzene at ice bath temperature. After the addition, the cooling bath was removed and the stirring continued for 24 hours. The reaction was cooled to ice bath temperature and a solution of piperidine (2.7 ml, 27.3 mmol) and pyridine (4.4 ml, 54.4 mmol) in 20 ml of benzene was added dropwise over 15 minutes. After the addition, the reaction was stirred at ice bath temperature for 3 hours. The cooling bath was removed and the stirring continued for 22 hours. The reaction was diluted with benzene and extracted two times with 1 N HCl. The organic solution was dried over anhydrous MgSO4 and the solvent was removed under reduced pressure to give 7.21 g of an oil. Purification by HPLC (hexane:EtOAc) gave 5.05 g of a light yellow crystalline solid. Recrystallization from diisopropyl ether gave the title compound as a white crystalline solid (3.11 g, 39%), mp 74°-76° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05512565
Source datasetuspto-grants-1996_04
ORD IDord-1d29375590aa4882a54235759de3905f
Source noteuspto-grants-1996_04