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Ethanol → 6-(4-Chloro-phenylsulfanyl)-hexylamine

HRID 2097362
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2097362
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([S:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14]C2C=CC=C3C(NC(=O)C=23)=O)=[CH:4][CH:3]=1.O.[NH2:27]N.CCO>C1COCC1>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([S:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][NH2:27])=[CH:6][CH:7]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 702EthanolHCID 24654Hydrazine hydrate (1:1)HCID 866225746-(4-Chlorophenylsulfanyl)-hexylphthalimide

Produkt 1

HCID 231324146-(4-Chloro-phenylsulfanyl)-hexylamine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

2-[6-(4-Chloro-phenylsulfanyl)-hexylphthalimide (7.47 g, 20 mmol) and hydrazine hydrate (6.1 ml, 100 mmol) were dissolved in THF (50 mL) and EtOH (50 mL) and stirred under reflux for 17 h. The solvent was removed under reduced pressure, the residue was suspended in THF (100 mL) and the precipitate was filtered off, washed with THF (1×50 mL) and the filtrate was concentrated under reduced pressure. The residue was resuspended in THF (25 mL), the precipitate was filtered off and the filtrate was concentrated to give the title compound.

Aufarbeitung

  1. temperatureunder reflux for 17 h
  2. customThe solvent was removed under reduced pressure
  3. filtrationthe precipitate was filtered off
  4. washwashed with THF (1×50 mL)
  5. concentrationthe filtrate was concentrated under reduced pressure
  6. filtrationthe precipitate was filtered off
  7. concentrationthe filtrate was concentrated

Quellen und Nachweise

ORD-Eintrag
ord-e9eeef1cc87e45759d828a2ceddda0c9
Quelldatensatz
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08450348B2

Notizen zur Reaktion

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