Reaktion #44880

ord-51017605c27a4df0905c4c42548db89d

Reaktionsgleichung

CC(C)(CCl)C(=O)Cl
3-chloropivaloyl chloride
OCc1ccccc1
benzyl alcohol
CCN(C(C)C)C(C)C
ethyldiisopropylamine
[I-].[Na+]
sodium iodide
CC(C)(C)OC(=O)NCC1CCNCC1
tert-butyl (piperidin-4-ylmethyl)carbamate
CC(C)(CCl)C(=O)OCc1ccccc1
benzyl 3-chloropivalate
CC(C)(C)OC(=O)NCC1CCN(CC(C)(C)C(=O)OCc2ccccc2)CC1
title compound
Ausbeute 1.3%
CC(C)(C)OC(=O)NCC1CCN(CC(C)(C)C(=O)OCc2ccccc2)CC1
tert-Butyl [{1-(2-benzyloxycarbonyl-2-methylpropyl)piperidin-4-yl}methyl]carbamate
Ausbeute 1.3%

Lösungsmittel

Reaktionsbedingungen

Temperatur
120°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe volatile components were removed by evaporation
  2. 2
    Sonstigethe resulting residue was chromatographed on a column of silica gel eluting with hexane/ethyl acetate (1:1)

Vorschrift

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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07737163B2uspto-grants-2010_06