Silver Nitrate → 4-(Nitrooxy)butanoic acid

HRID 1374691Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1374691
CC(C1C=C(SC(SC2C=C(C(C)(C)C)C([O:31][C:32](=[O:37])[CH2:33][CH2:34][CH2:35]Br)=C(C(C)(C)C)C=2)(C)C)C=C(C(C)(C)C)C=1O)(C)C.[N+:42]([O-:45])([O-:44])=[O:43].[Ag+]>C(#N)C.C1COCC1>[N+:42]([O:45][CH2:35][CH2:34][CH2:33][C:32]([OH:31])=[O:37])([O-:44])=[O:43]

Komponenten

4

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

To a solution of 4-bromobutanoic acid [4-[[1-[[3, 5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]thio]-1-methylethyl]thio]-2,6-bis(1,1-dimethylethyl)phenyl]ester (150 mg, 0.22 mmol) in acetonitrile/THF (15 ml 2/1 v/v), AgNO3 was added (80 mg, 0.47 mmol) and the solution was heated in the dark at 60° C. for 6 hours. The silver salt was then filtered off (AgBr) and the solvent was evaporated at reduced pressure. The product thus obtained was purified by chromatography on silica gel with a mixture of ethyl acetate/hexane as eluent (4/6 v/v) to give 4-nitrooxybutanoic acid, [4-[[1-[[3,5-bis(1,1-dimethyletihyl)-4-hydroxyphenyl]thio]-1-methylethyl]thio]-2,6-bis (1,1-dimethylethyl)-phenyl] ester (100 mg).

Aufarbeitung

  1. filtrationThe silver salt was then filtered off (AgBr)
  2. customthe solvent was evaporated at reduced pressure
  3. customThe product thus obtained
  4. customwas purified by chromatography on silica gel with a mixture of ethyl acetate/hexane as eluent (4/6 v/v)

Quellen und Nachweise

ORD-Eintrag
ord-453ab883dde1411e8d154dfa0b604362
Quelldatensatz
uspto-grants-2007_01
Patentnummer
US07166605B2

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