Carbon tetrabromide → 1-Bromo-5-(2-methoxyethoxy)methoxypentane

HRID 329521ノート

反応式

HRID 329521 の反応式
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[CH3:20][O:21][CH2:22][CH2:23][O:24][CH2:25][O:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31]O.C(Br)(Br)(Br)[Br:34]>C(Cl)Cl>[Br:34][CH2:31][CH2:30][CH2:29][CH2:28][CH2:27][O:26][CH2:25][O:24][CH2:23][CH2:22][O:21][CH3:20]

参加物

5

実験手順

79.32 g of triphenylphosphine were added, whilst ice-cooling (at 5° to 8° C.), to a solution of 48.40 g of 5-(2-methoxyethoxy)methoxy-1-pentanol (prepared as described in Preparation 59) and 100.19 g of carbon tetrabromide dissolved in 500 ml of methylene chloride. The mixture was stirred at room temperature for 1 hour, after which the solvent was removed by evaporation under reduced pressure. Diethyl ether was then added to the resulting residue. The insoluble materials were filtered off, and the filtrate was concentrated by evaporation under reduced pressure. The residue was subjected to column chromatography through 850 g of silica gel, and 57.87 g of the title compound were obtained, as a colorless oil, from those fractions eluted with a 1:9 by volume mixture of ethyl acetate and hexane.

後処理

  1. temperaturecooling (at 5° to 8° C.)
  2. customafter which the solvent was removed by evaporation under reduced pressure
  3. additionDiethyl ether was then added to the resulting residue
  4. filtrationThe insoluble materials were filtered off
  5. concentrationthe filtrate was concentrated by evaporation under reduced pressure

出典と根拠

ORDレコード
ord-3ad68c69837842ba93bfda9497e02e36
出典データセット
uspto-grants-1990_01
特許番号
US04891363

反応ノート

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