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Ethanol → 2-Methyl-4,5,6,7-tetrahydrobenzo[d]thiazole-7-carbonitrile

HRID 2371048
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2371048
[CH3:1][C:2]1[S:3][C:4]2[C:10](=O)[CH2:9][CH2:8][CH2:7][C:5]=2[N:6]=1.CC1C=CC(S([CH2:22][N+:23]#[C-])(=O)=O)=CC=1.C(O)C.CC([O-])(C)C.[K+]>COCCOC>[CH3:1][C:2]1[S:3][C:4]2[CH:10]([C:22]#[N:23])[CH2:9][CH2:8][CH2:7][C:5]=2[N:6]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 702EthanolHCID 161915Tosylmethyl isocyanideHCID 149133692-Methyl-5,6-dihydrobenzo[d]thiazol-7(4H)-oneHCID 23665647Potassium tert-butoxide

Produkt 1

HCID 672573622-Methyl-4,5,6,7-tetrahydrobenzo[d]thiazole-7-carbonitrile

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8071
1,2-Dimethoxyethane
Lösungsmittel

Versuchsvorschrift

To a stirred and cooled solution of 5,6-dihydro-2-methylbenzo[d]thiazol-7(4H)-one (1.67 g, 10 mmol) and TOSMIC (2.5 g, 13 mmol) in a mixture of DME (25 mL) and absolute ethanol (25 mL) was added solid t-BuOK (2.8 g, 24 mmol) portionwise while keeping the reaction temperature between 5 and 10° C. The resulting mixture was stirred at room temperature for 30 minutes and at 30-45° C. for 30 minutes. The resulting suspension was cooled to room temperature. The precipitate (TosK) was removed by filtration and rinsed with DME. The combined DME solutions were concentrated under reduced pressure to give the crude product, which was purified by column chromatography.

Aufarbeitung

  1. customthe reaction temperature between 5 and 10° C
  2. stirringThe resulting mixture was stirred at room temperature for 30 minutes and at 30-45° C. for 30 minutes
  3. customThe precipitate (TosK) was removed by filtration
  4. washrinsed with DME
  5. concentrationThe combined DME solutions were concentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-33190a766f104e7a9c9532481b7f2d87
Quelldatensatz
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08710245B2

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