Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hexamethylenetetramine | HCID 4101 | — |
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Phenacylamine | HCID 11952 | 106.9% |
Reaction Steps
2-Bromoacetophenone (18 g, 90 mmol) was dissolved in 900 m of chloroform. Hexamethylenetetraamine (13.87 g, 99 mmol) was added thereto and the reaction mixture was stirred at 60° C. for 4 hours. After stirring, the reaction mixture was cooled down to room temperature, filtered, and the collected precipitate was suspended in 180 m of ethanol. To the suspension thus obtained was added dropwise 90 m of conc. HCl, and the reaction mixture was stirred at room temperature for 18 hours. Then, the reaction mixture was filtered to remove a white precipitate, the filtrate was concentrated under reduced pressure to obtain a yellow solid. This solid was recrystallized from a mixture of methanol and ethyl acetate (1:50, v/v) to obtain 13 g of 2-aminoacetophenone as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05929103 |
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| Source dataset | uspto-grants-1999_07 |
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| ORD ID | ord-ea0b28de50524efbb0121fe8de00838f |
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| Source note | uspto-grants-1999_07 |
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