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Water → 1-[2-(Acetylamino)ethyl]-6-hydroxyindan

HRID 1978016
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1978016
[C:1]([NH:4][CH2:5][CH2:6][CH:7]1[C:15]2[C:10](=[CH:11][CH:12]=[C:13]([O:16]C)[CH:14]=2)[CH2:9][CH2:8]1)(=[O:3])[CH3:2].B(Br)(Br)Br.O>ClCCl>[C:1]([NH:4][CH2:5][CH2:6][CH:7]1[C:15]2[C:10](=[CH:11][CH:12]=[C:13]([OH:16])[CH:14]=2)[CH2:9][CH2:8]1)(=[O:3])[CH3:2]
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Komponenten

5

Edukt 3

HCID 962WaterHCID 25134Boron tribromideHCID 155239391-[2-(Acetylamino)ethyl]-6-methoxyindan

Produkt 1

HCID 219168881-[2-(Acetylamino)ethyl]-6-hydroxyindanAusbeute 78,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

To a solution of 1-[2-(acetylamino)ethyl]-6-methoxyindan (6.40 g, 27.4 mmol) in dichloromethane (150 ml) was added dropwise, under ice-cooling, boron tribromide (5.19 ml, 54.8 mmol). The mixture was then stirred for one hour. The reaction mixture was poured into water. The mixture was stirred for 8 hours at room temperature, which was subjected to extraction with chloroform. The extract solution was washed with brine, which was dried over anhydrous magnesium sulfate, followed by distilling off the solvent under reduced pressure. The residue was recrystallized from ethyl acetate/isopropyl ether to give 4.70 g (yield 78%) of the above-titled compound, m.p.107-108° C.

Aufarbeitung

  1. temperaturecooling
  2. stirringThe mixture was stirred for 8 hours at room temperature
  3. extractionwhich was subjected to extraction with chloroform
  4. washThe extract solution was washed with brine, which
  5. dry with materialwas dried over anhydrous magnesium sulfate
  6. distillationby distilling off the solvent under reduced pressure
  7. customThe residue was recrystallized from ethyl acetate/isopropyl ether

Quellen und Nachweise

ORD-Eintrag
ord-628e5fe3c26947a291469c14e60c6528
Quelldatensatz
uspto-grants-2001_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06235789B1

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