HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2-(Benzyloxy)-5-bromobenzaldehyde → (2-(Benzyloxy)-5-bromophenyl)methanol
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2-(Benzyloxy)-5-bromobenzaldehyde | HCID 733087 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | (2-(Benzyloxy)-5-bromophenyl)methanol | HCID 897136 | — |
Reaktionsschritte
A suspension of 2-benzyloxy-5-bromobenzaldehyde (14.5 g, 50.2 mmol) in absolute ethanol (250 ml) was treated with sodium borohydride (2.6 g, 68.8 mmol). The reaction was stirred and the temperature slowly rose to 33° C. After 1 hour the reaction mixture was evaporated and the residue dissolved in ethyl acetate and poured into a mixture of ice water (200 ml) and 1N HCl (25 ml). The organic layer was separated, washed with aqueous sodium hydrogen carbonate, brine, dried (Na2SO4) and evaporated to give 2-benzyloxy-5-bromobenzyl alcohol as a pale yellow oil (14.85 g, quantitative).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06313148B1 |
| Quelldatensatz | uspto-grants-2001_11 |
| ORD ID | ord-325e740b45744e5babf8867b57e39f40 |
| Quellennotiz | uspto-grants-2001_11 |