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Hydrochloric Acid → 3-(3-Methoxyphenyl)indoline

HRID 1489148
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1489148
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:9]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[NH:11][CH:10]=2)[CH:6]=[CH:7][CH:8]=1.Cl.[OH-].[Na+]>[Zn].C(O)C>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:9]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[NH:11][CH2:10]2)[CH:6]=[CH:7][CH:8]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 154287153-(3-Methoxyphenyl)indole

Produkt 1

HCID 154287243-(3-Methoxyphenyl)indolineAusbeute 48,6 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23994ZincKatalysatorHCID 702
Ethanol
Lösungsmittel

Versuchsvorschrift

Ten grams of the abovementioned 3-(3-methoxyphenyl)indole, 700 ml of 6N hydrochloric acid and 300 ml of ethanol were mixed and refluxed while 100 g zinc powder was added in small portions, and then the reflux was continued for 5 hours. The reaction solution was made alkaline with an aqueous sodium hydroxide solution and extracted with chloroform. The resultant extract solution was concentrated to a residue which was then dissolved in diluted hydrochloric acid, and washed with ether. The aqueous layer was made alkaline with sodium hydroxide, extracted with chloroform, and dried and concentrated to obtain 4.9 g of 3-(3-methoxyphenyl)indoline.

Aufarbeitung

  1. additionwas added in small portions
  2. extractionextracted with chloroform
  3. extractionThe resultant extract solution
  4. concentrationwas concentrated to a residue which
  5. dissolutionwas then dissolved in diluted hydrochloric acid
  6. washwashed with ether
  7. extractionextracted with chloroform
  8. customdried
  9. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-a8eafaad19b74b64894cde9c44c7ffbc
Quelldatensatz
uspto-grants-1997_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05677326

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