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Methanol → 2-(3,4-Dichlorophenyl)-3-hydroxy-4-methylcarbonyl-2,5-dihyrothiophene

HRID 1949133
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1949133
CO.[NH2-].[Na+].[Cl:5][C:6]1[CH:7]=[C:8]([CH:13]([S:18][CH2:19][CH2:20][C:21](=[O:23])[CH3:22])[C:14]([O:16]C)=O)[CH:9]=[CH:10][C:11]=1[Cl:12].[Cl-].[NH4+]>O>[Cl:5][C:6]1[CH:7]=[C:8]([CH:13]2[C:14]([OH:16])=[C:20]([C:21]([CH3:22])=[O:23])[CH2:19][S:18]2)[CH:9]=[CH:10][C:11]=1[Cl:12]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 887Methanol2×HCID 24533Sodium amideHCID 25517Ammonium ChlorideHCID 58281519Methyl 2-(3,4-dichlorophenyl)-2-(3-oxobutylthio)acetate

Produkt 1

HCID 442070402-(3,4-Dichlorophenyl)-3-hydroxy-4-methylcarbonyl-2,5-dihyrothiopheneAusbeute 69,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962
Water
Lösungsmittel

Reaktionsbedingungen

Temperatur
40 °C

Versuchsvorschrift

A methanol (500 mL) solution of sodium amide (19.2 g, purity: 90%, 1.5 equivalent amounts based on the starting material) was heated to 40° C., and to this solution, a methanol (200 mL) solution of methyl 2-(3,4-dichlorophenyl)-2-(3-oxobutylthio)acetate (100 g, purity: 95%, 296 mmol) was dropwise added over a period of 12 minutes, followed by stirring at 40° C. for 1 hour. The reaction solution was cooled to 5° C., water (300 mL) was dropwise added over a period of 10 minutes, and then the solvent was distilled off. To the obtained crude product, chloroform and a saturated ammonium chloride aqueous solution were added, followed by liquid separation, and the organic layer was washed with a saturated salt solution and dried over anhydrous magnesium sulfate. The drying agent was removed by filtration, and the solvent was distilled off to give the desired product as an oil (59.3 g, yield: 65%).

Aufarbeitung

  1. temperatureThe reaction solution was cooled to 5° C.
  2. distillationthe solvent was distilled off
  3. customTo the obtained crude product, chloroform
  4. customfollowed by liquid separation
  5. washthe organic layer was washed with a saturated salt solution
  6. dry with materialdried over anhydrous magnesium sulfate
  7. customThe drying agent was removed by filtration
  8. distillationthe solvent was distilled off

Quellen und Nachweise

ORD-Eintrag
ord-ab7b960c34b94f909af9147d38110052
Quelldatensatz
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08399685B2

Notizen zur Reaktion

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