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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176364Generated: October 30, 2026

Aminoacetaldehyde dimethyl acetal → 7,10-Di-tert-butyl-imidazo[1,2-f]phenanthridine

https://huagongshe.com/reaction/2176364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAminoacetaldehyde dimethyl acetalHCID 89728—
Reactant2,9-Di-tert-butyl-6-chlorophenanthridineHCID 57437659—
SolventDiglymeHCID 8150—
Product7,10-Di-tert-butyl-imidazo[1,2-f]phenanthridineHCID 5816236556%

Reaction Steps

2,9-Di-t-butyl-6-chlorophenanthridine (3.7 grams, 11.0 mmole) was added to a reaction flask containing aminoacetaldehyde dimethylacetal (2.4 grams, 23 mmole) dissolved into 200 mL of diglyme, heated to reflux and stirred under a nitrogen atmosphere. After 96 hours the reaction was complete as determined by TLC. The reaction mixture was cooled to room temperature and the excess solvent removed by distillation. The residue was taken up into methylene chloride. The solvent was dried over magnesium sulfate filtered and concentrated. The crude product was purified by silica gel chromatography using 10% ethyl acetate and 90% methylene chloride as the eluents. The purified product was collected, washed with hexanes, and dried to give 7,10-di-tert-butyl-imidazo[1,2-f]phenanthridine (2.0 grams, 56% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09065063B2
Source datasetuspto-grants-2015_06
ORD IDord-9b62230614b147b792e5419ee35af004
Source noteuspto-grants-2015_06