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Methyl 3-nitronaphthalene-1-carboxylate → Methyl 3-aminonaphthalene-1-carboxylate

HRID 1010619
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1010619
[N+:1]([C:4]1[CH:5]=[C:6]([C:14]([O:16][CH3:17])=[O:15])[C:7]2[C:12]([CH:13]=1)=[CH:11][CH:10]=[CH:9][CH:8]=2)([O-])=O>[Pd].C(O)C.ClCCl>[NH2:1][C:4]1[CH:5]=[C:6]([C:14]([O:16][CH3:17])=[O:15])[C:7]2[C:12]([CH:13]=1)=[CH:11][CH:10]=[CH:9][CH:8]=2
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 1

HCID 260948Methyl 3-nitronaphthalene-1-carboxylate

Produkt 1

HCID 23423661Methyl 3-aminonaphthalene-1-carboxylate

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 23938PalladiumKatalysatorHCID 702EthanolLösungsmittelHCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

To 1.15 g (1.08 mmol) of 10% palladium on carbon was added a suspension of 11.6 g (50.0 mmol) of the above methyl 3-nitro-1-naphthoate in 150 mL of anhydrous ethanol and 40 mL of anhydrous dichloromethane. The resulting suspension was agitated under an atmosphere of hydrogen at 40 psi for 3 h during which time all solids dissolved. The reaction mixture was filtered through a plug of Celite®, which was subsequently washed with dichloromethane (300 mL). The combined filtrates were concentrated in vacuo to yield the title compound as a pale green gum which was used without further purification. LC/MS 202.1 (N+1).

Aufarbeitung

  1. dissolutiondissolved
  2. filtrationThe reaction mixture was filtered through a plug of Celite®, which
  3. washwas subsequently washed with dichloromethane (300 mL)
  4. concentrationThe combined filtrates were concentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-2f5428bbba9943b8a3c4a0511f2032e5
Quelldatensatz
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07977339B2

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