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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291787Generated: October 31, 2026

Dimethylformamide → HCID 13730862, compound

https://huagongshe.com/reaction/2291787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantHCID 13339822HCID 13339822—
ReactantButyllithiumHCID 178418339—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
ProductHCID 13730862HCID 1373086278%

Reaction Conditions

Temperature-63 °C

Reaction Steps

To a mixture of 4-isopropyl-4-methyl-2-(2-quinolyl)-2-imidazolin-5-one (3 g, 0.0112 mol) in ether (150 ml) is added tetramethylethylenediamine (3.4 g, 0.00225 mol). n-Butyllithium (17 ml, 0.027 mol) in hexane is added dropwise to the reaction mixture cooled to -63° C. An intense red color is generated and after the addition the mixture was maintained at -10° to -20° C. for 21/2 hours. Dry DMF (5 ml) was added at -10° C. and the mixture is allowed to attain room temperature, while stirring overnight. The mixture is diluted with water (75 ml) and is neutralized with acetic acid. A pale yellow solid 2.57 g (78%) is obtained with mp 226°-227° C. after crystallization* from 95% ethanol. Anal. calcd. for C17H17N3O2 : C, 69.13; H, 5.80; N, 14.23. Found: C, 68.98; H, 5.88; N, 14.25. The oxime of this aldehyde, prepared in the usual way, has mp 255°-257° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04798619
Source datasetuspto-grants-1989_01
ORD IDord-aa5540cb8a3342f99b4ee9cd5c06b0d0
Source noteuspto-grants-1989_01