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Water → HCID 12819450, Verbindung

HRID 1277773
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1277773
CS[C:3]([C:9]1[CH:14]=[CH:13][C:12]([NH2:15])=[C:11]([Cl:16])[CH:10]=1)([CH3:8])[C:4]([O:6][CH3:7])=[O:5].O.C(OCC)C>C(O)(=O)C.[Zn].S([O-])([O-])(=O)=O.[Cu+2]>[Cl:16][C:11]1[CH:10]=[C:9]([CH:3]([CH3:8])[C:4]([O:6][CH3:7])=[O:5])[CH:14]=[CH:13][C:12]=1[NH2:15]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 3

HCID 962WaterHCID 3283Diethyl EtherHCID 12917666Methyl alpha-methylthio-alpha-(3-chloro-4-aminophenyl)propionate

Produkt 1

HCID 12819450HCID 12819450, VerbindungAusbeute 95,7 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 23994ZincKatalysator
HCID 24462
Copper Sulfate
Katalysator
HCID 176Acetic AcidLösungsmittel

Versuchsvorschrift

Methyl α-methylthio-α-(3-chloro-4-aminophenyl)propionate (380 mg) was dissolved in 4 ml of acetic acid, and an intimate mixture of 406 mg of zinc powder and 1.5 mg of anhydrous copper sulfate was added. The entire mixture was heated under reflux for 1 hour. Water (40 ml) and 15 ml of diethyl ether were added to the reaction mixture. The insoluble matter was separated by filtration, and then the organic layer was separated. Furthermore, the aqueous layer was extracted with 5 ml of diethyl ether. The organic layer and the extract were combined, washed with 15 ml of a saturated aqueous solution of sodium hydrogen carbonate, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to afford 299 mg of methyl α-(3-chloro-4-aminophenyl)propionate in a yield of 95.6% as a colorless oil.

Aufarbeitung

  1. additionwas added
  2. temperatureThe entire mixture was heated
  3. temperatureunder reflux for 1 hour
  4. customThe insoluble matter was separated by filtration
  5. customthe organic layer was separated
  6. extractionFurthermore, the aqueous layer was extracted with 5 ml of diethyl ether
  7. washwashed with 15 ml of a saturated aqueous solution of sodium hydrogen carbonate
  8. dry with materialdried over anhydrous magnesium sulfate
  9. concentrationconcentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-9035337a270a49b98fdece3c4dd1c968
Quelldatensatz
uspto-grants-1981_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04278802

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