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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442281Generated: October 30, 2026

3'-Aminoacetophenone → HCID 53797596, compound

https://huagongshe.com/reaction/442281

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3'-AminoacetophenoneHCID 7417—
Reactant(2,4-Bis(1,1-dimethylpropyl)phenoxy)acetyl chlorideHCID 66612—
SolventPyridineHCID 1049—
ProductHCID 53797596HCID 53797596—

Reaction Steps

40 grams (0.1 mol) of N-α -(2,4-di-tert-amylphenoxy)acetyl-m-aminoacetophenone (m.p.:135° C), obtained by the reaction between m-aminoacetophenone and α-(2,4-di-tert-amylphenoxy)acetyl chloride in pyridine, was dissolved in 200 ml of anhydrous ethyl ether (placed in a three-necked flask), and 0.5 g of anhydrous aluminum chloride powder was added to this solution followed by ice-cooling (about 0°-5° C.) under stirring. 16 grams (0.1 mol) of bromine was added dropwise to this mixture. After the completion of the dropwise addition, the temperature was allowed to rise to room temperature (about 20°-35° C.). Stirring was continued until the generation of hydrogen bromide stopped. Thus, white crystals were precipitated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE029379
Source datasetuspto-grants-1977_08
ORD IDord-5743cc92a7824857ab15dd0fdd0e8ac4
Source noteuspto-grants-1977_08