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Sodium Hydroxide → 4-[(1-Methyl-1H-tetrazol-5-yl)sulfanyl]butanoic acid

HRID 2290232
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2290232
C([O:3][C:4](=[O:15])[CH2:5][CH2:6][CH2:7][S:8][C:9]1[N:13]([CH3:14])[N:12]=[N:11][N:10]=1)C.[OH-].[Na+]>C1COCC1>[CH3:14][N:13]1[C:9]([S:8][CH2:7][CH2:6][CH2:5][C:4]([OH:15])=[O:3])=[N:10][N:11]=[N:12]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 14798Sodium HydroxideHCID 21295546HCID 21295546, Verbindung

Produkt 1

HCID 130916224-[(1-Methyl-1H-tetrazol-5-yl)sulfanyl]butanoic acid

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

2.93 g of 4-(1-methyltetrazol-5-ylthio)-butyric acid ethyl ester are dissolved in 50 ml of THF, 15 ml of 1N NaOH are added and the whole is stirred for 3 hours at room temperature. Most of the THF is then concentrated by evaporation under reduced pressure in a rotary evaporator and the residue is washed with ethyl acetate. The aqueous solution is adjusted to pH 3 with 4N HCl and extracted three times with ethyl acetate. After drying over sodium sulphate and concentration by evaporation under reduced pressure, the pure title compound is obtained.

Aufarbeitung

  1. concentrationMost of the THF is then concentrated by evaporation under reduced pressure in a rotary evaporator
  2. washthe residue is washed with ethyl acetate
  3. extractionextracted three times with ethyl acetate
  4. dry with materialAfter drying over sodium sulphate and concentration by evaporation under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-8c68a04d750d416e8995293d97712081
Quelldatensatz
uspto-grants-1986_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04616007

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