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Diiodomethane → HCID 22292780, Verbindung

HRID 967260
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 967260
[CH2:1]([Zn]CC)[CH3:2].FC(F)(F)C(O)=O.ICI.[F:16][C:17]([F:35])([F:34])[C:18]([N:20]1[CH2:26][C:25](=[CH2:27])[C:24]2[CH:28]=[CH:29][C:30]([O:32][CH3:33])=[CH:31][C:23]=2[CH2:22][CH2:21]1)=[O:19]>ClCCl>[F:35][C:17]([F:16])([F:34])[C:18]([N:20]1[CH2:26][CH:25]([CH:27]2[CH2:2][CH2:1]2)[C:24]2[CH:28]=[CH:29][C:30]([O:32][CH3:33])=[CH:31][C:23]=2[CH2:22][CH2:21]1)=[O:19]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 6346DiiodomethaneHCID 6422Trifluoroacetic acidHCID 22292788N-Trifluoroacetyl-7-methoxy-1-methylene 2,3,4,5-tetrahydro-1H-3-benzazepineHCID 178418750HCID 178418750, Verbindung

Produkt 1

HCID 22292780HCID 22292780, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344
Dichloromethane
Lösungsmittel
4×

Versuchsvorschrift

A solution of diethyl zinc (1 mL, 1 M in hexanes) in dichloromethane (1 mL) at 0 C. was treated with trifluoroacetic acid in dichloromethane (0.5 mL) and the mixture stirred for 15 min. Diiodomethane (0.280 g, 1.0 mmol) in dichloromethane (0.5 mL) was then added and stirred for 15 minutes. N-Trifluoroacetyl-7-methoxy-1-methylene-2,3,4,5-tetrahydro-1H-3-benzazepine (0.075 g, 0.26 mmol) in dichloromethane (1 mL) was added and the mixture stirred for 30 minutes at 0 C. and then for 2 hours at 20 C. The product mixture was quenched with aqueous saturated NH4Cl (5 mL), extracted twice with CH2Cl2 (20 mL), washed with saturated aqueous NaHCO3 (10 mL), washed with H2O (10 mL), and concentrated. Flash chromatography (7% EtOAc in hexanes, silica) resulted in 0.050 g of a white solid. MS calculated for C15H16F3NO2+H: 300, observed: 300.

Aufarbeitung

  1. stirringstirred for 15 minutes
  2. stirringthe mixture stirred for 30 minutes at 0 C
  3. waitand then for 2 hours at 20 C
  4. customThe product mixture was quenched with aqueous saturated NH4Cl (5 mL)
  5. extractionextracted twice with CH2Cl2 (20 mL)
  6. washwashed with saturated aqueous NaHCO3 (10 mL)
  7. washwashed with H2O (10 mL)
  8. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-eb84b8f65b904b00aa416ca1c4335dbf
Quelldatensatz
uspto-grants-2005_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06953787B2

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