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Cyclopropanecarboxylic acid 4-chloro-3-hydroxymethyl-benzylamide → Cyclopropanecarboxylic Acid 4-chloro-3-formyl-benzylamide

HRID 2428136
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2428136
[Cl:1][C:2]1[CH:14]=[CH:13][C:5]([CH2:6][NH:7][C:8]([CH:10]2[CH2:12][CH2:11]2)=[O:9])=[CH:4][C:3]=1[CH2:15][OH:16]>CC#N.O=[Mn]=O>[Cl:1][C:2]1[CH:14]=[CH:13][C:5]([CH2:6][NH:7][C:8]([CH:10]2[CH2:11][CH2:12]2)=[O:9])=[CH:4][C:3]=1[CH:15]=[O:16]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 1

HCID 67148310Cyclopropanecarboxylic acid 4-chloro-3-hydroxymethyl-benzylamide

Produkt 1

HCID 86632362Cyclopropanecarboxylic Acid 4-chloro-3-formyl-benzylamideAusbeute 94,1 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 14801Manganese dioxideKatalysator3×HCID 6342AcetonitrileLösungsmittel

Versuchsvorschrift

MnO2 (6.29 g, 72.0 mmol) was added to a sol. of cyclopropanecarboxylic acid 4-chloro-3-hydroxymethyl-benzylamide (3.47 g, 14.0 mmol) in CH3CN (300 mL) at rt. The mixture was stirred for 3 h at rt, and MnO2 (2.52 g, 29.0 mmol) was added again. The mixture was stirred for 1 h at rt, and MnO2 (1.26 g, 14.0 mmol) was added again. The mixture was stirred for 1.5 h, and was filtered through celite. The filtrate was evaporated under reduced pressure, and the residue was dried under high vacuum to yield the crude title compound (3.13 g, 91%) that was used further without purification. LC-MS: tR=0.80 min; ES+: 279.31.

Aufarbeitung

  1. stirringThe mixture was stirred for 1 h at rt
  2. stirringThe mixture was stirred for 1.5 h
  3. filtrationwas filtered through celite
  4. customThe filtrate was evaporated under reduced pressure
  5. customthe residue was dried under high vacuum

Quellen und Nachweise

ORD-Eintrag
ord-e40a95dcfb6343469488598a3c7562c6
Quelldatensatz
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07968720B2

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