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N-(4-Chloro-3-hydroxymethyl-benzyl)-3,3,3-trifluoro-propionamide → N-(4-Chloro-3-formyl-benzyl)-3,3,3-trifluoro-propionamide

HRID 2428104
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2428104
[Cl:1][C:2]1[CH:16]=[CH:15][C:5]([CH2:6][NH:7][C:8](=[O:14])[CH2:9][C:10]([F:13])([F:12])[F:11])=[CH:4][C:3]=1[CH2:17][OH:18]>CC#N.O=[Mn]=O>[Cl:1][C:2]1[CH:16]=[CH:15][C:5]([CH2:6][NH:7][C:8](=[O:14])[CH2:9][C:10]([F:13])([F:12])[F:11])=[CH:4][C:3]=1[CH:17]=[O:18]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 1

HCID 67148258N-(4-Chloro-3-hydroxymethyl-benzyl)-3,3,3-trifluoro-propionamide

Produkt 1

HCID 86622955N-(4-Chloro-3-formyl-benzyl)-3,3,3-trifluoro-propionamideAusbeute 100,5 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 14801Manganese dioxideKatalysator2×HCID 6342AcetonitrileLösungsmittel

Versuchsvorschrift

MnO2 (1.44 g, 14.9 mmol) was added to a sol. of N-(4-chloro-3-hydroxymethyl-benzyl)-3,3,3-trifluoro-propionamide (841 mg, 2.99 mmol) in CH3CN (60 mL). The mixture was stirred at rt for 3 h. MnO2 (1.44 g, 14.9 mmol) was added again, and the mixture was stirred for 90 min. The mixture was filtered over celite, and the precipitate was washed with CH3CN and CH2Cl2. The solvents were removed under reduced pressure, and the residue was dried under high vacuum, yielding the crude title compound (840 mg, quantitative yield) that was used further without purification. LC-MS: tR=0.84 min; ES+: 341.21.

Aufarbeitung

  1. stirringthe mixture was stirred for 90 min
  2. filtrationThe mixture was filtered over celite
  3. washthe precipitate was washed with CH3CN and CH2Cl2
  4. customThe solvents were removed under reduced pressure
  5. customthe residue was dried under high vacuum

Quellen und Nachweise

ORD-Eintrag
ord-86c8171dae35482a8dca06e8c5f4d18b
Quelldatensatz
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07968720B2

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