Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 597548Erstellt: 25. Oktober 2026

Benzyl Bromide → 4-Piperidinol, 2,2,6,6-tetramethyl-1-(phenylmethyl)-

https://huagongshe.com/reaction/597548

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
Edukt4-Hydroxy-2,2,6,6-tetramethylpiperidineHCID 75471—
LösungsmittelEthanolHCID 702—
Produkt4-Piperidinol, 2,2,6,6-tetramethyl-1-(phenylmethyl)-HCID 103602—

Reaktionsschritte

A mixture of 31.4 parts of 2,2,6,6-tetramethylpiperidin-4-ol and 17.1 parts of benzyl bromide in 125 parts of ethyl alcohol was heated under reflux conditions for 96 hours. The cooled reaction mixture was filtered to remove 2,2,6,6-tetramethylpiperidin-4-ol hydrobromide formed during the reaction and the ethyl alcohol solvent was removed by distillation under reduced pressure. Purification of the residue by chromatography on a aluminia column using chloroform as the solvent gave 1-benzyl-2,2,6,6-tetramethylpiperidin-4-ol having a melting point of 151°-2°C and the following elemental analysis by weight

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04014887
Quelldatensatzuspto-grants-1977_03
ORD IDord-fabf840c398a4b41a2b3105305022d47
Quellennotizuspto-grants-1977_03