Reaktion #7309

ord-53c4bad16d5f4bd785263b5a0042463c

Reaktionsgleichung

CC1CCNCC1
4-methylpiperdine
CCN(CC)CC
triethylamine
COC(=O)Cl
methylchloroformate
O
water
COC(=O)N1CCC(C)CC1
product
COC(=O)N1CCC(C)CC1
4-Methyl-piperidine-1-carboxylic acid methyl ester

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe mixture was cooled in an ice bath
  2. 2
    Sonstigethe layers were separated
  3. 3
    WaschenThe organic layer was washed with dilute HCl
  4. 4
    TrocknenNaHCO3, and brine, and then the organic layer was dried over sodium sulfate
  5. 5
    Sonstigethe solvent was removed in vacuo
  6. 6
    workup.DISTILLATIONThe product was distilled at 90-93 C at ˜10 mm pressure

Vorschrift

To a three neck round bottom flask was added 360 g of 4-methylpiperdine, 470 mL of triethylamine, and 390 mL of methylene chloride and the mixture was cooled in an ice bath. To this mixture was added methylchloroformate (260 mL) in methylene chloride (215 mL) slowly to maintain a reaction temperature of 20 C or below. The reaction was stirred overnight, then 200 mL of water was added and the layers were separated. The organic layer was washed with dilute HCl, satd. NaHCO3, and brine, and then the organic layer was dried over sodium sulfate and the solvent was removed in vacuo. The product was distilled at 90-93 C at ˜10 mm pressure to provide 338 g of product.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07084277B2uspto-grants-2006_08