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Water → HCID 19909372, Verbindung

HRID 2073225
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2073225
[NH2-].[Na+].[C:3]1([CH2:13][C:14]#[N:15])[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH:6]=[CH:5][CH:4]=1.[CH2:16]([CH:23]1[CH2:28][CH2:27][N:26]([CH2:29][CH2:30]Cl)[CH2:25][CH2:24]1)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1.O>CCOCC>[CH2:16]([CH:23]1[CH2:28][CH2:27][N:26]([CH2:29][CH2:30][CH:13]([C:3]2[C:12]3[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=3)[CH:6]=[CH:5][CH:4]=2)[C:14]#[N:15])[CH2:25][CH2:24]1)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 962WaterHCID 85961-NaphthaleneacetonitrileHCID 24533Sodium amideHCID 15870313HCID 15870313, Verbindung

Produkt 1

HCID 19909372HCID 19909372, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3283Diethyl EtherLösungsmittel

Versuchsvorschrift

2 g of sodium amide are added in small portions to a solution of naphth-1-ylacetonitrile in 150 ml of anhydrous ether and the mixture is refluxed for 5 hours. 11.8 g of 2-(4-benzylpiperidino)chloroethane are then added and the mixture is refluxed again for 3.5 hours. 200 ml of water are added and the organic phase is decanted and extracted with 300 ml of 10% hydrochloric acid. The aqueous phase is washed with ether, neutralized with 30% sodium hydroxide and extracted with ether. The organic phase is washed with a saturated aqueous solution of sodium chloride and dried over magnesium sulfate and the solvent is then evaporated off to give 16.4 g of the expected product.

Aufarbeitung

  1. temperaturethe mixture is refluxed for 5 hours
  2. temperaturethe mixture is refluxed again for 3.5 hours
  3. customthe organic phase is decanted
  4. extractionextracted with 300 ml of 10% hydrochloric acid
  5. washThe aqueous phase is washed with ether
  6. extractionextracted with ether
  7. washThe organic phase is washed with a saturated aqueous solution of sodium chloride
  8. dry with materialdried over magnesium sulfate
  9. customthe solvent is then evaporated off

Quellen und Nachweise

ORD-Eintrag
ord-6a39b645ea0d4457877fbe4e7111c2b6
Quelldatensatz
uspto-grants-1990_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04916156

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