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HCID 12262631, Verbindung → 3-Methoxy-6,7,8,9-tetrahydro-5H-benzo[7]annulen-6-one

HRID 274079
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 274079
N[CH2:2][C:3]1([OH:15])[C:12]2[C:7](=[CH:8][CH:9]=[C:10]([O:13][CH3:14])[CH:11]=2)[CH2:6][CH2:5][CH2:4]1.N([O-])=O.[Na+]>C(O)(=O)C.O>[CH3:14][O:13][C:10]1[CH:9]=[CH:8][C:7]2[CH2:6][CH2:5][CH2:4][C:3](=[O:15])[CH2:2][C:12]=2[CH:11]=1
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Komponenten

5

Edukt 2

HCID 12262631HCID 12262631, VerbindungHCID 23668193Sodium Nitrite

Produkt 1

HCID 105595743-Methoxy-6,7,8,9-tetrahydro-5H-benzo[7]annulen-6-oneAusbeute 76,8 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 176Acetic AcidLösungsmittelHCID 962WaterLösungsmittel

Versuchsvorschrift

To a solution of 1-aminomethyl-7-methoxy-1,2,3,4-tetrahydro-1-naphthalenol (27.50 g) in 10% aqueous acetic acid solution (250 ml) was added dropwise a solution of sodium nitrite (10.07 g) in water (61 ml) at 8° C.~9° C. The reaction mixture was stirred for 2 hours at the same temperature. The resulting precipitates were collected by filtration. The precipitates were dissolved in ethyl acetate. The solution was dried over magnesium sulfate and evaporated in vacuo. The residue was purified by column chromatography (silica gel, n-hexane:ethyl acetate:chloroform=5:1:3) to give 3-methoxy-6,7,8,9-tetrahydro-5H-benzocyclohepten-6-one (19.39 g) as a white powder.

Aufarbeitung

  1. customThe resulting precipitates
  2. filtrationwere collected by filtration
  3. dissolutionThe precipitates were dissolved in ethyl acetate
  4. dry with materialThe solution was dried over magnesium sulfate
  5. customevaporated in vacuo
  6. customThe residue was purified by column chromatography (silica gel, n-hexane:ethyl acetate:chloroform=5:1:3)

Quellen und Nachweise

ORD-Eintrag
ord-9dda68e7336240aaa16a72cc41678acc
Quelldatensatz
uspto-grants-1995_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05387710

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