Hexane → 2-(2-Bromoethyl)naphthalene

HRID 247171

Reaktionsgleichung

Reaktionsgleichung von HRID 247171
[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[CH2:11][CH2:12]O.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[Br:33]N1C(=O)CCC1=O.CCCCCC>C1C=CC=CC=1>[Br:33][CH2:12][CH2:11][C:2]1[CH:3]=[CH:4][C:5]2[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=2)[CH:1]=1

Komponenten

6

Edukt 4

HCID 8058HexaneHCID 11776TriphenylphosphineHCID 67184N-bromobutanimideHCID 738772-Naphthaleneethanol

Produkt 1

HCID 2282702-(2-Bromoethyl)naphthalene

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 241BenzeneLösungsmittel

Versuchsvorschrift

To a solution of 25 g (145 mmole) of 2-(2-naphthyl)ethanol and 67.9 g (259 mmole) of triphenylphosphine in 200 ml of benzene was added in portions 46.1 g (259 mmole) of N-bromosuccinimide. A temperature of 45°-50° was maintained by cooling the reaction mixture as needed in an ice bath. After the mixture was poured into 750 ml of hexane and filtered, the filtrate was diluted with an additional 400 ml of hexane and allowed to stand overnight. The solution was concentrated to dryness and the resultant solid was purified by chromatography on silica gel. The title compound (30.5 g), m.p. 55°-57°, was homogeneous by thin-layer chromatography (5%, 10%, and 15% by volume ethyl acetate-hexane on silica gel plates), and was used in subsequent reactions without further purification.

Aufarbeitung

  1. temperatureA temperature of 45°-50° was maintained
  2. temperatureby cooling the reaction mixture
  3. customas needed in an ice bath
  4. filtrationfiltered
  5. additionthe filtrate was diluted with an additional 400 ml of hexane
  6. concentrationThe solution was concentrated to dryness
  7. customthe resultant solid was purified by chromatography on silica gel
  8. customwas used in subsequent reactions without further purification

Quellen und Nachweise

ORD-Eintrag
ord-1d1d1f7f77a34b1881cbc2ec43fabba6
Quelldatensatz
uspto-grants-1987_11
Patentnummer
US04705871

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