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Sodium Hydroxide → 1,2,3,4-Tetrahydro-benzo(b)azepin-5-one

HRID 220778
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 220778
C1(C)C=CC(S([N:10]2[CH2:16][CH2:15][CH2:14][C:13](=[O:17])[C:12]3[CH:18]=[CH:19][CH:20]=[CH:21][C:11]2=3)(=O)=O)=CC=1.[OH-].[Na+]>>[NH:10]1[CH2:16][CH2:15][CH2:14][C:13](=[O:17])[C:12]2[CH:18]=[CH:19][CH:20]=[CH:21][C:11]1=2
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 14798Sodium HydroxideHCID 2668521-Tosyl-3,4-dihydro-1H-benzo[b]azepin-5(2H)-one

Produkt 1

HCID 2947881,2,3,4-Tetrahydro-benzo(b)azepin-5-oneAusbeute 79 %

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

Polyphosphoric acid (25 g) was heated at 100° C. under nitrogen until it could be stirred. 1-(Toluene-4-sulfonyl)-1,2,3,4-tetrahydro-benzo[b]azepin-5-one from Example E5.4 (2.6 g, 8.26 mmol) was added portionwise and the reaction mixture was heated at 100° C. for 1.5 h. It was poured into ice and basified with 2M NaOH(aq). The aqueous layer was extracted twice with dichloromethane. The organic extracts were combined, washed with brine, dried and reduced in vacuo. The residue was purified by flash chromatography on silica gel (eluant; 40% EtOAc:60% hexane) to yield the title compound (1.05 g, 79%).

Aufarbeitung

  1. additionIt was poured into ice
  2. extractionThe aqueous layer was extracted twice with dichloromethane
  3. washwashed with brine
  4. customdried
  5. customThe residue was purified by flash chromatography on silica gel (eluant; 40% EtOAc:60% hexane)

Quellen und Nachweise

ORD-Eintrag
ord-241a1209b347432fbfe0d168bba0df6d
Quelldatensatz
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08202858B2

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