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Hydrochloric Acid → Benzyl 2-amino-2-methylpropanoate hydrochloride

HRID 230925
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 230925
C(OC([NH:8][C:9]([CH3:21])([CH3:20])[C:10]([O:12][CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)=[O:11])=O)(C)(C)C.[ClH:22]>C(OCC)C>[ClH:22].[NH2:8][C:9]([CH3:21])([CH3:20])[C:10]([O:12][CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)=[O:11]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 313Hydrochloric AcidHCID 23077832Tert-butyl 2-((benzyloxy)carbonyl)propan-2-ylcarbamate

Produkt 1

HCID 21415531Benzyl 2-amino-2-methylpropanoate hydrochloride

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3283Diethyl EtherLösungsmittel

Versuchsvorschrift

To a solution of 2-(tert-butoxycarbonylamino)-2-methylpropionic acid (4.06 g) in N,N-dimethylformamide (40 mL) were added potassium carbonate (4.15 g) and benzyl bromide (2.85 mL), and the mixture was stirred at room temperature for 2 hours. The reaction mixture was poured into water, and the resulting mixture was extracted with ethylacetate. The extract was washed with water and brine, and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure. The residue (solid) was treated with n-hexane and collected by filtration. The crystals were dried under reduced pressure to give benzyl 2-(tert-butoxycarbonylamino)-2-methylpropionate (4.44 g). To the obtained benzyl 2-(tert-butoxycarbonylamino)-2-methylpropionate (4.44 g) was added 4 mol/L hydrochloric acid (1,4-dioxane solution, 15 mL), and the mixture was stirred at room temperature overnight. The reaction mixture was diluted with diethyl ether, and the mixture was stirred for 1 hour. The insoluble material was collected by filtration, washed with diethyl ether and dried under reduced pressure to give the title compound (3.4 g).

Aufarbeitung

  1. stirringthe mixture was stirred for 1 hour
  2. filtrationThe insoluble material was collected by filtration
  3. washwashed with diethyl ether
  4. customdried under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-3108d3fe5d494e348c081fabef4ee3d8
Quelldatensatz
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07566699B2

Notizen zur Reaktion

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