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Tert-Butylamine → Carbamate

HRID 1992335
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1992335
Cl[C:2](Cl)([O:4][C:5](=[O:11])OC(Cl)(Cl)Cl)Cl.[C:13]([NH2:17])([CH3:16])([CH3:15])[CH3:14].C(N(CC)CC)C.[Br:25][CH2:26][CH2:27][OH:28]>C(Cl)Cl.CN(C1C=CN=CC=1)C.O>[C:5](=[O:11])([O-:4])[NH2:17].[C:13]([NH:17][C:2](=[O:4])[O:28][CH2:27][CH2:26][Br:25])([CH3:16])([CH3:15])[CH3:14]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

9

Edukt 4

HCID 6385Tert-ButylamineHCID 8471TriethylamineHCID 108982-BromoethanolHCID 94429Triphosgene

Produkt 2

HCID 276CarbamateHCID 179479972-Bromoethyl tert-butylcarbamate

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 14284
4-(Dimethylamino)pyridine
Katalysator
HCID 962WaterLösungsmittel
HCID 6344DichloromethaneLösungsmittel2×

Versuchsvorschrift

To a cooled solution of triphosgene (76 g, 0.256 mol, 0.75 eq.) in dry DCM (150 mL) was added, dropwise at 0° C. over a period of 3 hrs under a N2 atmosphere, a mixture of tert-butylamine (25 g, 0.3418 mol, 1.0 eq.), DMAP (2.08 g, 0.017 mol, 0.05 eq.) and triethylamine (67.1 g, 0.6836 mol, 2.0 eq.) in dry DCM (100 mL). After addition of the mixture was complete, the reaction mixture was stirred at RT for 12 hrs. The reaction mixture was cooled to 0° C. and 2-bromoethanol (106.8 g, 0.854 mol, 2.5 eq.) was added. The reaction mixture was then stirred at RT for 6 hrs, before being diluted with water and extracted with DCM. The combined organic layers were washed with brine, dried over anhydrous Na2SO4, and then concentrated under reduced pressure. The resulting residue was distilled under reduced pressure to yield carbamate the sub-title compound as a colourless liquid. Yield: 28 g.

Aufarbeitung

  1. additionAfter addition of the mixture
  2. temperatureThe reaction mixture was cooled to 0° C.
  3. stirringThe reaction mixture was then stirred at RT for 6 hrs
  4. extractionextracted with DCM
  5. washThe combined organic layers were washed with brine
  6. dry with materialdried over anhydrous Na2SO4
  7. concentrationconcentrated under reduced pressure
  8. distillationThe resulting residue was distilled under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-2d81cabefa5d445ea9318b972dfb4ec8
Quelldatensatz
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07648985B2

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