Hexane → 2-(2-Bromoethyl)naphthalene

HRID 247171

反応式

HRID 247171 の反応式
[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

参加物

6

反応物 4

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

生成物 1

HCID 2282702-(2-Bromoethyl)naphthalene

試薬・触媒・溶媒 1

HCID 241Benzene溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-1d1d1f7f77a34b1881cbc2ec43fabba6
出典データセット
uspto-grants-1987_11
特許番号
US04705871

関連ノート

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