1,4'-Bipiperidine → 1-Chlorocarbonyl-4-piperidinopiperidine hydrochloride

HRID 1444682

Reaktionsgleichung

Reaktionsgleichung von HRID 1444682
[Cl:1][C:2](Cl)([O:4]C(=O)OC(Cl)(Cl)Cl)Cl.[N:13]1([CH:19]2[CH2:24][CH2:23][NH:22][CH2:21][CH2:20]2)[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1>C(Cl)Cl>[ClH:1].[N:13]1([CH:19]2[CH2:24][CH2:23][N:22]([C:2]([Cl:1])=[O:4])[CH2:21][CH2:20]2)[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1

Komponenten

4

Edukt 2

HCID 786071,4'-BipiperidineHCID 94429Triphosgene2×

Produkt 1

HCID 116375531-Chlorocarbonyl-4-piperidinopiperidine hydrochloride

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel2×

Versuchsvorschrift

Triphosgene (100 g) was dissolved in 1280 ml of methylene chloride. Solution of 129.5 g of 4-piperidinopiperidine was dissolved in 1280 ml of methylene chloride and this solution was added at 20-25° C. into the triphosgene solution while cooling the mixture (exothermic reaction). Part of the methylene chloride (1500 ml) was distilled off. Acetonitrile (580 ml) was added gradually. Methylene chloride was distilled off until the temperature rose to 63° C. Toluene (2000 ml) was added gradually. The mixture was cooled to room temperature. The crystalline compound was filtered and washed with toluene (about 1000 ml). The compound was dried under reduced pressure at about 40° C.

Aufarbeitung

  1. temperaturewhile cooling
  2. customthe mixture (exothermic reaction)
  3. distillationPart of the methylene chloride (1500 ml) was distilled off
  4. additionAcetonitrile (580 ml) was added gradually
  5. distillationMethylene chloride was distilled off until the temperature
  6. customrose to 63° C
  7. additionToluene (2000 ml) was added gradually
  8. filtrationThe crystalline compound was filtered
  9. washwashed with toluene (about 1000 ml)
  10. customThe compound was dried under reduced pressure at about 40° C.

Quellen und Nachweise

ORD-Eintrag
ord-d39e083a16d44fc68bdc71a8fc6452c5
Quelldatensatz
uspto-grants-2010_02
Patentnummer
US07662964B2

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