Acetic Anhydride → HCID 21401618, Verbindung

HRID 1730139Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1730139
[OH:1][CH:2]([CH2:20][O:21][C:22]1[CH:27]=[CH:26][C:25]([F:28])=[CH:24][CH:23]=1)[CH2:3][CH2:4][CH2:5][N:6]([CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][C:17]([OH:19])=[O:18])[S:7]([CH3:10])(=[O:9])=[O:8].[C:29](OC(=O)C)(=[O:31])[CH3:30]>C(OCC)C>[C:29]([O:1][CH:2]([CH2:20][O:21][C:22]1[CH:27]=[CH:26][C:25]([F:28])=[CH:24][CH:23]=1)[CH2:3][CH2:4][CH2:5][N:6]([CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][C:17]([OH:19])=[O:18])[S:7]([CH3:10])(=[O:9])=[O:8])(=[O:31])[CH3:30]

Komponenten

4

Versuchsvorschrift

A mixture of 7-{N-[4-hydroxy-5-(4-fluorophenoxy)-pentyl]methanesulfonamido}heptanoic acid (12.3 g., 0.03 mole) (Example 1, Step E) and acetic anhydride (6.1 g., 0.06 mole) is kept at room temperature for 18 hours. This mixture is taken up in 80 ml. of ethyl ether. The solution is extracted with an ice-cold solution of 8 g. of sodium hydroxide in 150 ml. of water. The basic solution is separated and acidified with concentrated hydrochloric acid. The crude product that separates is extracted into ether, washed with water and dried over sodium sulfate. The ether is evaporated and the residual oil is purified by chromatography on silica gel using 2% methanol in chloroform as the eluting solvent. There is obtained 7-{N-[4-acetoxy-5-(4-fluorophenoxy)pentyl]methanesulfonamido}-heptanoic acid as a viscous oil.

Aufarbeitung

  1. extractionThe solution is extracted with an ice-cold solution of 8 g
  2. customThe basic solution is separated
  3. extractionThe crude product that separates is extracted into ether
  4. washwashed with water
  5. dry with materialdried over sodium sulfate
  6. customThe ether is evaporated
  7. customthe residual oil is purified by chromatography on silica gel using 2% methanol in chloroform as the eluting solvent

Quellen und Nachweise

ORD-Eintrag
ord-dcda1aeb2f104c4ca2e7257d280909c8
Quelldatensatz
uspto-grants-1976_11
Patentnummer
US03991106

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