HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(1-Azidotridecyl)-2-triethylsilylfuran → 4-(1-Aminotridecyl)-2-triethylsilylfuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(1-Azidotridecyl)-2-triethylsilylfuran | HCID 19433146 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Product | 4-(1-Aminotridecyl)-2-triethylsilylfuran | HCID 15037086 | — |
Reaction Steps
Reacting 4-(1-hydroxytridecyl)-2-trimethylsilylfuran with diphenylphosphonyl azide and diethyl azidocarboxylate gives 4-(1-azidotridecyl)-2-triethylsilylfuran. Reducing this azide with lithium aluminum hydride gives 4-(1-aminotridecyl)-2-triethylsilylfuran. Acetylation of this intermediate with acetic anhydride gives 4-(1-acetamido)tridecyl-2-triethylsilylfuran. Oxidizing this amide with oxygen using Rose Bengal as an initiator gives 4-(1-acetamido)-5-hydroxy-2(5H)-furanone. Reduction of this furanone with sodium borohydride gives 4-(1-acetamido)-2(5H)-furanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05376676 |
| Source dataset | uspto-grants-1994_12 |
| ORD ID | ord-5523ed214df44af4a26b63e748fea057 |
| Source note | uspto-grants-1994_12 |