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Hydrochloric Acid → (3-Chloro-4-methylsulfanyl-phenyl)-oxo-acetic acid

HRID 398679
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 398679
C[O:2][C:3](=[O:15])[C:4]([C:6]1[CH:11]=[CH:10][C:9]([S:12][CH3:13])=[C:8]([Cl:14])[CH:7]=1)=[O:5].[OH-].[Na+].Cl>C1(C)C=CC=CC=1>[Cl:14][C:8]1[CH:7]=[C:6]([C:4](=[O:5])[C:3]([OH:15])=[O:2])[CH:11]=[CH:10][C:9]=1[S:12][CH3:13]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 12069497(3-Chloro-4-methylsulfanyl-phenyl)-oxo-acetic acid methyl ester

Produkt 1

HCID 12067649(3-Chloro-4-methylsulfanyl-phenyl)-oxo-acetic acidAusbeute 98,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1140TolueneLösungsmittel

Reaktionsbedingungen

Temperatur
50 °C

Versuchsvorschrift

A solution of (3-chloro-4-methylsulfanyl-phenyl)-oxo-acetic acid methyl ester (61.7 g, 252 mmol) in toluene (120 mL) was heated at 50° C. This heated solution was then treated dropwise with a 3M aqueous sodium hydroxide solution (105 mL, 313 mmol) via a dropping funnel, taking care to keep the temperature below 60° C. After the addition was complete, the reaction mixture was stirred at 50° C. for another 1.5 h, during which time, a yellow precipitate began to form. After this time, the heat was removed, and the warm solution was treated dropwise with concentrated hydrochloric acid (10.6 mL, 290 mmol). The resulting reaction mixture was allowed to cool to 25° C. and then was stirred at 25° C. for 16 h. The solid was filtered and then washed with water (50 mL) and toluene (50 mL). The solid was dried by suction for 1 h and then dried in a high vacuum desiccator to afford (3-chloro-4-methylsulfanyl-phenyl)-oxo-acetic acid (57.22 g, 98%) as a white solid: mp 166° C. (dec); FAB-HRMS m/e calcd for C9H7ClSO3 (M+Na)+ 252.9702, found 252.9700.

Aufarbeitung

  1. customthe temperature below 60° C
  2. additionAfter the addition
  3. customto form
  4. customAfter this time, the heat was removed
  5. customThe resulting reaction mixture
  6. temperatureto cool to 25° C.
  7. stirringwas stirred at 25° C. for 16 h
  8. filtrationThe solid was filtered
  9. washwashed with water (50 mL) and toluene (50 mL)
  10. customThe solid was dried by suction for 1 h
  11. customdried in a high vacuum desiccator

Quellen und Nachweise

ORD-Eintrag
ord-02e8cfe40a40471a95bef84bd10ff0b1
Quelldatensatz
uspto-grants-2003_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06610846B1

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