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llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
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Hydrazine hydrate (1:1) → (Z)-7-Aminohept-5-enoic Acid

HRID 358624
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 358624
O.NN.C1(=O)[N:8]([CH2:9]/[CH:10]=[CH:11]\[CH2:12][CH2:13][CH2:14][C:15]([OH:17])=[O:16])C(=O)C2=CC=CC=C12>C(O)C.O>[NH2:8][CH2:9]/[CH:10]=[CH:11]\[CH2:12][CH2:13][CH2:14][C:15]([OH:17])=[O:16]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 24654Hydrazine hydrate (1:1)HCID 67946768(Z)-7-Phthalimidohept-5-enoic Acid

Produkt 1

HCID 86744642(Z)-7-Aminohept-5-enoic AcidAusbeute 112,7 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 702EthanolLösungsmittelHCID 962WaterLösungsmittel

Versuchsvorschrift

Hydrazine hydrate (0.19 ml) was added to a solution of (Z)-7-phtalimidohept-5-enoic acid (1.05 g) in ethanol (25 ml) and water (5 ml). The solution was refluxed for 3 hours and then the solvent was removed. The residue was suspended in water and the pH of the solution was adjusted to 5. The resulting precipitate was collected by filtration. The filtrate was evaporated to dryness and extracted with ethanol. The ethanol extracts were evaporated to dryness to give the title compound as an oil (0.62 g).

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Aufarbeitung

  1. temperatureThe solution was refluxed for 3 hours
  2. customthe solvent was removed
  3. filtrationThe resulting precipitate was collected by filtration
  4. customThe filtrate was evaporated to dryness
  5. extractionextracted with ethanol
  6. customThe ethanol extracts were evaporated to dryness

Quellen und Nachweise

ORD-Eintrag
ord-8e756c3c47864deebc89d4eb381cda53
Quelldatensatz
uspto-grants-1991_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04997847

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