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Hydrochloric Acid → 1-(1,2-Diamino-1-methylethyl)-1-cyclopropanecarboxylate dihydrochloride

HRID 1510343
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1510343
[NH2:1][C:2]([C:6]1([C:9]([O:11]C(C)(C)C)=[O:10])[CH2:8][CH2:7]1)([CH3:5])[CH2:3][NH2:4].O.[ClH:17]>>[ClH:17].[ClH:17].[NH2:1][C:2]([C:6]1([C:9]([OH:11])=[O:10])[CH2:7][CH2:8]1)([CH3:5])[CH2:3][NH2:4]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 313Hydrochloric AcidHCID 962WaterHCID 57434367Tert-butyl 1-(1,2-diamino-1-methylethyl)-1-cyclopropanecarboxylate

Produkt 1

HCID 574343681-(1,2-Diamino-1-methylethyl)-1-cyclopropanecarboxylate dihydrochloride

Versuchsvorschrift

0.82 g (3.83 mmol) of the crude tert-butyl 1-(1,2-diamino-1-methyl ethyl)-1-cyclopropanecarboxylate was dissolved in concentrated hydrochloric acid (5 mL) at room temperature, and the solution was stirred at the same temperature for 30 minutes. After adding water to the reaction solution, the solvent was removed by distillation under reduced pressure. The residue was azeotropically distilled with ethanol (twice) to obtain 0.82 g (3.55 mmol, 93%) of the crude target compound as a pale yellow foam solid. The thus obtained crude product was used in the subsequent reaction with no further purification.

Aufarbeitung

  1. customthe solvent was removed by distillation under reduced pressure
  2. distillationThe residue was azeotropically distilled with ethanol (twice)
  3. customto obtain 0.82 g (3.55 mmol, 93%) of the crude target compound as a pale yellow foam solid
  4. customThe thus obtained crude product
  5. customwas used in the subsequent reaction with no further purification

Quellen und Nachweise

ORD-Eintrag
ord-d78f1a5a4ef64d79a5180f81b35c576e
Quelldatensatz
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08211910B2

Notizen zur Reaktion

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