Phosgene → (4,4-Diethoxybutyl)carbamic acid 5-chloro-pentyl ester

HRID 10185

Reaktionsgleichung

Reaktionsgleichung von HRID 10185
[C:1](Cl)(Cl)=[O:2].[Cl:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][OH:11].C(N(CC)C1C=CC=CC=1)C.[CH2:23]([O:25][CH:26]([O:31][CH2:32][CH3:33])[CH2:27][CH2:28][CH2:29][NH2:30])[CH3:24].C(N(CC)CC)C>C1(C)C=CC=CC=1.C(OCC)(=O)C>[Cl:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][O:11][C:1](=[O:2])[NH:30][CH2:29][CH2:28][CH2:27][CH:26]([O:25][CH2:23][CH3:24])[O:31][CH2:32][CH3:33]

Komponenten

8

Versuchsvorschrift

To an ice-cooled solution of 1.93M phosgene in toluene (31 mL, 60 mmole) was added dropwise a solution of 5-chloro-1-pentanol (4.9 g, 40 mmole) and N,N-diethylaniline (5.97 g, 40 mmole) in toluene (40 mL). The reaction mixture was stirred at ambient temperature for 4 hours. The mixture was filtered, and the filtrate was concentrated. The residue was taken up in ethyl acetate, filtered, and the solution was added dropwise to an ice-cooled solution of 4-aminobutyraldehyde diethylacetal (7.09 g, 44 mmole) and triethylamine (4.45 g, 44 mmole) in ethyl acetate (60 mL). The reaction mixture was stirred at room temperature for 15 hours, filtered and concentrated. Purification by silica gel chromatography, eluting with 10% ethyl acetate in hexane, gave (4,4-diethoxybutyl)carbamic acid 5-chloro-pentyl ester (11.4 g,) as an oil.

Aufarbeitung

  1. filtrationThe mixture was filtered
  2. concentrationthe filtrate was concentrated
  3. filtrationfiltered
  4. additionthe solution was added dropwise to an ice-
  5. stirringThe reaction mixture was stirred at room temperature for 15 hours
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customPurification by silica gel chromatography
  9. washeluting with 10% ethyl acetate in hexane

Quellen und Nachweise

ORD-Eintrag
ord-9a5e82ef097e4629a01e8536961e61b4
Quelldatensatz
uspto-grants-2006_08
Patentnummer
US07094778B2

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