HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1637755Erstellt: 26. Oktober 2026
Sodium borohydride → 1-(Isoquinolin-1-yl)ethan-1-ol
https://huagongshe.com/reaction/1637755
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | 1-(Isoquinolin-1-yl)ethan-1-one | HCID 13157214 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 1-(Isoquinolin-1-yl)ethan-1-ol | HCID 12337920 | 98,2% |
Reaktionsschritte
1-Acetyl-isoquinoline (2.0 g, 11.7 mmole) is dissolved in 50 ml methanol in a 100 ml one neck round bottom flask at 0° C. The solution is treated portionwise with sodium borohydride (495 mg, 13.1 mmole) and the reaction mixture is stirred for 1 h at 0° C. The volatiles are removed in vacuo and the residue is partitioned between 1×50 ml 1N sodium hydroxide and 4×25 ml dichloromethane. The combined organics are dried over potassium carbonate and are concentrated in vacuo to a pale oil. The crude material is chromatographed over 100 g silica gel (230-400 mesh), eluting with 15% acetone/hexane, while collecting 22 ml fractions. Fractions 23-37 are combined and concentrated to afford 1.99 g (98%) of 1-(1-hydroxyethyl)-isoquinoline.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06043248 |
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| Quelldatensatz | uspto-grants-2000_03 |
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| ORD ID | ord-a59bda8bf05643ceaf94bd9098fc1648 |
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| Quellennotiz | uspto-grants-2000_03 |
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