HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
P-Chloroacetophenone → p-Chlorophenacyl bromide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | P-Chloroacetophenone | HCID 7467 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Produkt | p-Chlorophenacyl bromide | HCID 68303 | — |
| Produkt | 2-Amino-1-(4-chlorophenyl)ethan-1-one hydrochloride | HCID 2798211 | — |
Reaktionsschritte
The starting 2-amino-1-(4-chlorophenyl)ethanone hydrochloride was prepared according to the following procedure. The 1-(4-chlorophenyl)ethanone (1.0 eq.) was dissolved in glacial acetic acid (1 ml, per mmol). To this was added a slurry of pyridinium bromide perbromide (1.03 eq.) in acetic acid (1 mL per mmol). The heterogeneous mixture was stirred for 4 h at ambient temperature. After about 30 min. the mixture turned homogeneous. After pouring into ice-water a yellow precipitate was filtered off and washed with water (2×1 mL per mmol of starting ketone). Drying of the precipitate afforded 2-bromo-1-(4-chlorophenyl)ethanone in ca. 90% yield.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08017555B2 |
| Quelldatensatz | uspto-grants-2011_09 |
| ORD ID | ord-c36b39ac91384ba699e4e403ccd48175 |
| Quellennotiz | uspto-grants-2011_09 |