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Pyridine → 7-chloro-3,4-dihydro-2H-naphthalen-1-one-O-methyl-oxime

HRID 241503
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 241503
[Cl:1][C:2]1[CH:11]=[C:10]2[C:5]([CH2:6][CH2:7][CH2:8][C:9]2=O)=[CH:4][CH:3]=1.N1C=CC=CC=1.Cl.[CH3:20][O:21][NH2:22]>CO>[CH3:20][O:21][N:22]=[C:9]1[C:10]2[C:5](=[CH:4][CH:3]=[C:2]([Cl:1])[CH:11]=2)[CH2:6][CH2:7][CH2:8]1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 1049PyridineHCID 2566777-Chloro-1,2,3,4-tetrahydronaphthalen-1-oneHCID 521874O-Methylhydroxylamine hydrochloride

Produkt 1

HCID 866998767-chloro-3,4-dihydro-2H-naphthalen-1-one-O-methyl-oximeAusbeute 100 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Reaktionsbedingungen

Temperatur
24 °C

Versuchsvorschrift

To a stirred solution of 7-chloro-1-tetralone CAS: 26673-32-5 (5.0 g; 27.68 mmol) in methanol (55 ml) was added pyridine (2.87 ml; 34.05 mmol) followed by a portion wise addition of methoxyamine hydrochloride (2.84 g; 34.05 mmol). The reaction mixture was stirred at 24° C. for 16 h under nitrogen. Methanol was removed under reduced pressure, the residue poured in water (300 ml) and 1N hydrochloric acid was added (100 ml). The solution was extracted with dichloromethane (3×150 ml). Combined organic layers were washed with water (300 ml) and dried over sodium sulfate. The solvent was removed in vacuo to afford 6.22 g (100% of theory) of crude 7-chloro-3,4-dihydro-2H-naphthalen-1-one-O-methyl-oxime as a brown oil.

Aufarbeitung

  1. customMethanol was removed under reduced pressure
  2. additionthe residue poured in water (300 ml)
  3. addition1N hydrochloric acid was added (100 ml)
  4. extractionThe solution was extracted with dichloromethane (3×150 ml)
  5. washCombined organic layers were washed with water (300 ml)
  6. dry with materialdried over sodium sulfate
  7. customThe solvent was removed in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-d23521188cca4cfaab81244a486e6095
Quelldatensatz
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08653003B2

Notizen zur Reaktion

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