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Methyl 3-(1-((tert-butoxycarbonyl)amino)ethyl)benzoate → Methyl 3-(1-aminoethyl)benzoate

HRID 1255834
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1255834
C(OC([NH:8][CH:9]([C:11]1[CH:12]=[C:13]([CH:18]=[CH:19][CH:20]=1)[C:14]([O:16][CH3:17])=[O:15])[CH3:10])=O)(C)(C)C>FC(F)(F)C(O)=O.ClCCl>[NH2:8][CH:9]([C:11]1[CH:12]=[C:13]([CH:18]=[CH:19][CH:20]=1)[C:14]([O:16][CH3:17])=[O:15])[CH3:10]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 1

HCID 68656133Methyl 3-(1-((tert-butoxycarbonyl)amino)ethyl)benzoate

Produkt 1

HCID 19933442Methyl 3-(1-aminoethyl)benzoateAusbeute 100,7 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6344DichloromethaneLösungsmittelHCID 6422Trifluoroacetic acidLösungsmittel

Versuchsvorschrift

A solution of methyl 3-{1-[(tert-butoxycarbonyl)amino]ethyl}benzoate (200 mg, 0.72 mmol) in 20% trifluoroacetic acid in dichloromethane (10 mL) was stirred at room temperature for 1.5 hours. After this time the mixture was concentrated under reduced pressure and the residue was dissolved in water and basified to pH 11 with aqueous ammonia. The mixture was extracted with ethyl acetate (2×15 mL) and the extracts were washed with brine (20 mL), dried (Na2SO4) and concentrated under reduced pressure to give methyl 3-(1-aminoethyl)benzoate (130 mg, 100%) as a pale yellow oil.

Aufarbeitung

  1. concentrationAfter this time the mixture was concentrated under reduced pressure
  2. dissolutionthe residue was dissolved in water and basified to pH 11 with aqueous ammonia
  3. extractionThe mixture was extracted with ethyl acetate (2×15 mL)
  4. washthe extracts were washed with brine (20 mL)
  5. dry with materialdried (Na2SO4)
  6. concentrationconcentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-f999f13fc8ee473c8a84b583daf83d99
Quelldatensatz
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08461161B2

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