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N-Iodosuccinimide → 5-Iodoindolin-2-one

HRID 457624
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 457624
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][C:2]1=[O:10].[I:11]N1C(=O)CCC1=O>C(O)(=O)C>[I:11][C:6]1[CH:5]=[C:4]2[C:9](=[CH:8][CH:7]=1)[NH:1][C:2](=[O:10])[CH2:3]2
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 120273N-IodosuccinimideHCID 321710Oxindole

Produkt 1

HCID 98380455-Iodoindolin-2-oneAusbeute 58 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 176Acetic AcidLösungsmittel

Reaktionsbedingungen

Temperatur
10 °C

Versuchsvorschrift

2-Oxindole (82.9 g) was suspended in 630 mL of acetic acid with mechanical stirring and the mixture cooled to 10° C. in an ice water bath. Solid N-iodosuccinimide (175 g) was added in portions over 10 minutes. After the addition was complete the mixture was stirred for 1.0 hour at 10° C. The suspended solid which had always present became very thick at this time. The solid was collected by vacuum filtration, washed with 100 mL of 50% acetic acid in water and then with 200 mL of water and sucked dry for 20 minutes in the funnel. The product was dried under vacuum to give 93.5 g (36%) of 5-iodo-2-oxindole containing about 5% 2-oxindole by proton NMR.

Aufarbeitung

  1. additionAfter the addition
  2. stirringwas stirred for 1.0 hour at 10° C
  3. filtrationThe solid was collected by vacuum filtration
  4. washwashed with 100 mL of 50% acetic acid in water
  5. dry with materialwith 200 mL of water and sucked dry for 20 minutes in the funnel
  6. customThe product was dried under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-0c4daf25cc0446c3b1ceff3514247e00
Quelldatensatz
uspto-grants-2007_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07189721B2

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