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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609576Generated: October 31, 2026

N,N-Dimethylaniline → HCID 53939820, compound

https://huagongshe.com/reaction/1609576

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
ReactantPyridineHCID 1049—
ReactantDiphosgeneHCID 10426—
ReactantOctodrineHCID 10982—
Reactant2-DibenzofuranolHCID 66587—
SolventBenzeneHCID 241—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 53939820HCID 53939820130.3%

Reaction Steps

A solution of 2-hydroxydibenzofuran (5.0 g, 27 mmol) and dimethylaniline (3.4 mL, 27 mmol) in 35 mL of benzene plus 1.5 mL of dioxane was added dropwise under nitrogen to a solution of trichloromethyl chloroformate (1.6 mL, 14 mmol) in 30 mL of benzene at ice bath temperature. After the addition the cooling bath was removed and the stirring continued for approximately 24 hours. The reaction was cooled to ice bath temperature and a solution of 1,5-dimethylhexylamine (4.6 mL, 27 mmol) and pyridine (4.4 mL, 54 mmol) in 30 mL of benzene was added dropwise over 15 minutes. After the addition the reaction was stirred at ice bath temperature for 2 hours. The cooling bath was removed and the stirring continued for approximately 22 hours. The reaction was extracted two times with 1N HCl. The organic solution was dried over anhydrous MgSO4 and the solvent removed under reduced pressure to give 6.19 g of a yellow solid. Recrystallization from isopropanol gave 4.27 g (46%) of the title compound as a yellow crystalline solid, mp 114°-115° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05401769
Source datasetuspto-grants-1995_03
ORD IDord-606c7fde20c64b2d969872aa39a406a9
Source noteuspto-grants-1995_03