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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 16602Erstellt: 26. Oktober 2026

Benzyl Alcohol → tert-Butyl [{1-(2-benzyloxycarbonyl-2-methylpropyl)piperidin-4-yl}methyl]carbamate

https://huagongshe.com/reaction/16602

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl AlcoholHCID 244—
EduktSodium IodideHCID 5238—
Edukt3-Chloro-2,2-dimethylpropanoyl chlorideHCID 61345—
EduktDiisopropylethylamineHCID 81531—
EduktTert-butyl (piperidin-4-ylmethyl)carbamateHCID 723429—
EduktBenzyl 3-chloropivalateHCID 54294282—
LösungsmittelDimethylformamideHCID 6228—
Produkttert-Butyl [{1-(2-benzyloxycarbonyl-2-methylpropyl)piperidin-4-yl}methyl]carbamateHCID 866021211,3%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

To a stirred solution of tert-butyl (piperidin-4-ylmethyl)carbamate (38.8 g, 181 mmol) in N,N-dimethylformamide (100 mL) was added benzyl 3-chloropivalate {14.2 g, 124 mmol, prepared from 3-chloropivaloyl chloride (25.6 g, 165 mmol) and benzyl alcohol (19.6 g, 181 mmol), ethyldiisopropylamine (64.0 g, 495 mmol) and sodium iodide (27.1 g, 181 mmol) at ambient temperature. The resulting mixture was stirred at 120° C. for 14 h. The volatile components were removed by evaporation and the resulting residue was chromatographed on a column of silica gel eluting with hexane/ethyl acetate (1:1) to give 640 mg (1%) of the title compound as a pale yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737163B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-51017605c27a4df0905c4c42548db89d
Quellennotizuspto-grants-2010_06