Iodoethane → 2-Benzyloxycarbonylamino-4-carbamoyl-butyric acid ethyl ester

HRID 2088330

Reaktionsgleichung

Reaktionsgleichung von HRID 2088330
[CH2:1]([O:8][C:9]([NH:11][CH:12]([CH2:16][CH2:17][C:18](=[O:20])[NH2:19])[C:13]([OH:15])=[O:14])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(=O)(O)[O-].[Na+].[CH2:26](I)[CH3:27]>O>[CH2:26]([O:14][C:13](=[O:15])[CH:12]([NH:11][C:9]([O:8][CH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)=[O:10])[CH2:16][CH2:17][C:18](=[O:20])[NH2:19])[CH3:27]

Komponenten

5

Edukt 3

HCID 6340IodoethaneHCID 3024262-(((Benzyloxy)carbonyl)amino)-4-carbamoylbutanoic acidHCID 516892Sodium Bicarbonate

Produkt 1

HCID 140366882-Benzyloxycarbonylamino-4-carbamoyl-butyric acid ethyl esterAusbeute 66,9 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

A mixture of acid (1) (64 g, 0.228 mol), dimeththylformamide (210 ml) and sodium bicarbonate (111 g, 1.32 mol, 5.8 equiv.) was stirred at room temperature for 30 min. Ethyl iodide (34 ml, 66.3 g, 0.425 mol, 1.86 equiv.) was added and stirring was continued overnight under nitrogen. The reaction mixture was slowly diluted with water to 1 L and stirred for 40 min. The solid was collected by filtration, washed well with water and partitioned between ethyl acetate (8 L) and water (3 L). Phases were separated and the aqueous phase was extracted with ethyl acetate (2.5 L). The combined organic extracts were washed with water (1 L), dried over sodium sulfate, stripped and dried in a vacuum oven (50° C.) to produce (2) (47 g, 66.7%).

Aufarbeitung

  1. stirringstirring
  2. waitwas continued overnight under nitrogen
  3. stirringstirred for 40 min
  4. filtrationThe solid was collected by filtration
  5. washwashed well with water
  6. custompartitioned between ethyl acetate (8 L) and water (3 L)
  7. customPhases were separated
  8. extractionthe aqueous phase was extracted with ethyl acetate (2.5 L)
  9. washThe combined organic extracts were washed with water (1 L)
  10. dry with materialdried over sodium sulfate
  11. customdried in a vacuum oven (50° C.)

Quellen und Nachweise

ORD-Eintrag
ord-979cc2040f5d404dbb3b3238f49b1c41
Quelldatensatz
uspto-grants-2013_05
Patentnummer
US08435956B2

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