HuagongsheHuagongshe Chemistry Print Report · For research reference only
3'-Aminoacetophenone → HCID 53797596, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3'-Aminoacetophenone | HCID 7417 | — |
| Reactant | (2,4-Bis(1,1-dimethylpropyl)phenoxy)acetyl chloride | HCID 66612 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 53797596 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE029379 |
| Source dataset | uspto-grants-1977_08 |
| ORD ID | ord-5743cc92a7824857ab15dd0fdd0e8ac4 |
| Source note | uspto-grants-1977_08 |