HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1019000Erstellt: 26. Oktober 2026
Imidazole → Tert-butyl 4-iodopiperidine-1-carboxylate
https://huagongshe.com/reaction/1019000
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Imidazole | HCID 795 | — |
| Edukt | Iodine | HCID 807 | — |
| Edukt | Triphenylphosphine | HCID 11776 | — |
| Edukt | Tert-butyl 4-hydroxypiperidine-1-carboxylate | HCID 643502 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | Tert-butyl 4-iodopiperidine-1-carboxylate | HCID 10892302 | — |
Reaktionsschritte
86 g of iodine are added at ambient temperature to a suspension of 89 g of triphenylphosphine and 22 g of imidazole in 800 ml of acetonitrile. The reaction is exothermic. After return to ambient temperature, 45.9 g of the product obtained in Step 1 in 250 ml of acetonitrile are added in the course of 30 minutes. After 18 hours' stirring at ambient temperature, the reaction mixture is filtered and rinsed with 200 ml of acetonitrile and the resulting filtrate is concentrated in vacuo. The residue obtained is stirred in 250 ml of diethyl ether for 1 hour and the precipitate is filtered off. After concentration of the filtrate in vacuo, chromatography on silica gel (dichloromethane/ethyl acetate: 90/10) enables the expected product to be isolated.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US06486171B2 |
|---|
| Quelldatensatz | uspto-grants-2002_11 |
|---|
| ORD ID | ord-bf2d29da904a4c639c0b64cfd009a431 |
|---|
| Quellennotiz | uspto-grants-2002_11 |
|---|