Iodoacetic Acid → 2-benzoylsulfanylacetic Acid

HRID 342331

Reaktionsgleichung

Reaktionsgleichung von HRID 342331
[C:1]([OH:9])(=[S:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH-].[K+].I[CH2:13][C:14]([OH:16])=[O:15]>C(O)C.O>[C:1]([S:8][CH2:13][C:14]([OH:16])=[O:15])(=[O:9])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Komponenten

6

Edukt 3

HCID 5240Iodoacetic AcidHCID 14797Potassium HydroxideHCID 178526132HCID 178526132, Verbindung

Produkt 1

HCID 51165332-benzoylsulfanylacetic AcidAusbeute 99 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 702EthanolLösungsmittel3×HCID 962WaterLösungsmittel

Versuchsvorschrift

To a purged stirring solution at 0° C. of (5.74 g, 41.6 mmoles) thiobenzoic acid in (100 mL) ethanol was added (27.8 mL, 3N, 83.2 mmoles) potassium hydroxide followed by (7.70 g, 41.6 mmoles) iodoacetic acid in (30 mL) ethanol. The solution stirred for 10 hours at room temperature under argon. The ethanol was rotavapped and the orange solid product was dissolved in (40 mL) water. The solution was acidified to pH 2.0 where an orange precipitate formed. This was filtered, washed with water, and dried in vacuo to give (7.98 g, 99% yield) benzoylmercaptoacetic acid.

Aufarbeitung

  1. customformed
  2. filtrationThis was filtered
  3. washwashed with water
  4. customdried in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-3e014ac0b5e042538bd993422686bacb
Quelldatensatz
uspto-grants-1999_01
Patentnummer
US05858327

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