tert-butyl N-[2-(2-benzyloxy-4-isopropylphenyl)ethyl]carbamate → 2-(2-Benzyloxy-4-isopropylphenyl)ethylamine hydrochloride

HRID 1351776Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1351776
[CH2:1]([O:8][C:9]1[CH:14]=[C:13]([CH:15]([CH3:17])[CH3:16])[CH:12]=[CH:11][C:10]=1[CH2:18][CH2:19][NH:20]C(=O)OC(C)(C)C)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(O)C.[ClH:31]>C(O)C>[ClH:31].[CH2:1]([O:8][C:9]1[CH:14]=[C:13]([CH:15]([CH3:17])[CH3:16])[CH:12]=[CH:11][C:10]=1[CH2:18][CH2:19][NH2:20])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Komponenten

4

Edukt 2

HCID 18457007tert-butyl N-[2-(2-benzyloxy-4-isopropylphenyl)ethyl]carbamateHCID 21887872Ethanol hydrochloride

Produkt 1

HCID 178562292-(2-Benzyloxy-4-isopropylphenyl)ethylamine hydrochloride

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

To a solution of 0.300 g of tert-butyl N-[2-(2-benzyloxy-4-isopropylphenyl)ethyl]carbamate in 2 mL of ethanol was added 2 mL of 21% hydrogen chloride ethanol solution at room temperature. After being stirred at the same temperature for 2 hours, the reaction mixture was concentrated under reduced pressure to give 0.261 g of 2-(2-benzyloxy-4-isopropylphenyl)ethylamine hydrochloride.

Aufarbeitung

  1. concentrationthe reaction mixture was concentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-488e6f459a8b489d8acf829ae3b49827
Quelldatensatz
uspto-grants-2007_05
Patentnummer
US07217832B2

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