HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Ethanone, 1-(3,5-bis(phenylmethoxy)phenyl)- → 1-(3,5-Bis(phenylmethoxy)phenyl)-2-bromoethan-1-one
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Ethanone, 1-(3,5-bis(phenylmethoxy)phenyl)- | HCID 120098 | — |
| Edukt | Tetra-n-butylammonium tribromide | HCID 23500184 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 1-(3,5-Bis(phenylmethoxy)phenyl)-2-bromoethan-1-one | HCID 120097 | — |
Reaktionsschritte
To a stirred solution of 1-[3,5-bis(benzyloxy)phenyl]ethanone (5 g, 15.04 mmol) in tetrahydrofuran (60 mL) and methanol (35 mL) was added tetrabutylammonium tribromide (7.25 g, 15.04 mmol) in tetrahydrofuran (20 mL) at room temperature. The reaction mixture was stirred for 24 hours and the solvent removed in vacuo. The residue was dissolved in ethyl acetate (100 mL) and washed with water (2×50 mL). The combined organic extracts were dried over magnesium sulfate and concentrated to afford the desired compound as a yellow oil in quantitative yield.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07538141B2 |
| Quelldatensatz | uspto-grants-2009_05 |
| ORD ID | ord-37b82bc9545047b0916a4cec67c3ded1 |
| Quellennotiz | uspto-grants-2009_05 |