HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 278248Erstellt: 25. Oktober 2026
Triethylamine → 4-Piperidinemethanol, 1-benzoyl-
https://huagongshe.com/reaction/278248
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Isobutyl chloroformate | HCID 62365 | — |
| Edukt | 1-Benzoylpiperidine-4-carboxylic acid | HCID 78935 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 4-Piperidinemethanol, 1-benzoyl- | HCID 10262870 | 99,2% |
Reaktionsschritte
To a solution of 2 g of 1-benzoylisonipecotic acid (Step A) in 50 mL THF at 0° C. were added 1.47 g of triethylamine and 1.99 g of isobutyl chloroformate. The reaction was stirred for 1 h at 0° C. To a solution of 1.10 g of sodium borohydride in 30 mL DMF at 0° C. was slowly added the above THF mixture. The reaction was again stirred for 1 h at 0° C. Water (80 mL) was slowly added to the reaction and the mixture was extracted 5×80 mL ethyl acetate and the combined organic layers were dried over magnesium sulfate. The solvent was then evaporated under reduced pressure. The residue was purified by flash chromatography with 1:1 hexane : ethyl acetate followed by hexane : ethyl acetate: methanol, 50:50:5 to give 1.865 g of the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US06358979B1 |
|---|
| Quelldatensatz | uspto-grants-2002_03 |
|---|
| ORD ID | ord-ac9768a399e142d29cfd64358aaa3407 |
|---|
| Quellennotiz | uspto-grants-2002_03 |
|---|