HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Sodium borohydride → Benzenemethanol,2-benzo[b]thien-5-yl-
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | Benzaldehyde,2-benzo[b]thien-5-yl- | HCID 60139760 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | Benzenemethanol,2-benzo[b]thien-5-yl- | HCID 60139743 | 93,7% |
Reaktionsschritte
To a suspension of 2-Benzo[b]thiophene-5-yl-benzaldehyde (compound PRE14) (3.31 g, 13.9 mmole) in methanol (30 mL) was added at 0-5° C. portionwise NaBH4 (0.528 g, 13.9 mmole). At the end of the addition, the cooling bath was removed and the reaction mixture was stirred at room temperature for 2 h. After concentration, the residue was diluted with water and diethyl ether, the organic layer dried over Na2SO4 and concentrated to give 3.13 g of compound O7 as an orange brown oil (Yield=94%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07449481B2 |
| Quelldatensatz | uspto-grants-2008_11 |
| ORD ID | ord-019cd25709ee4712a39f89c9e7b44b58 |
| Quellennotiz | uspto-grants-2008_11 |