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3-Bromobenzaldehyde → 1-Bromo-3-(2-methyl-1-propenyl)benzene

HRID 1594944
ノート
印刷プレビュー

反応式

HRID 1594944 の反応式
[I-].[CH:2]([P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)([CH3:4])[CH3:3].C([Li])CCC.[Br:29][C:30]1[CH:31]=[C:32]([CH:35]=[CH:36][CH:37]=1)[CH:33]=O>C1COCC1>[CH:33]([C:32]1[CH:31]=[C:30]([Br:29])[CH:37]=[CH:36][CH:35]=1)=[C:2]([CH3:4])[CH3:3]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 765833-BromobenzaldehydeHCID 2723783Isopropyltriphenylphosphonium iodideHCID 178418339Butyllithium

生成物 1

HCID 217068361-Bromo-3-(2-methyl-1-propenyl)benzene収率 79%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
-23 °C

実験手順

To a suspension of iso-propyltriphenylphosphonium iodide in dry THF (150 mL) under nitrogen at −23° C. was added 2.5 M n-butyl lithium in hexanes (13.4 mL, 33.6 mmol). The resulting solution was stirred 0.5 hours at −23° C., the cooling bath was removed, and the reaction was stirred 0.5 hours at ambient temperature to give a dark red homogeneous solution which was cooled to −23° C. To the solution was added neat 3-bromobenzaldehyde (3.73 mL, 32 mmol). The cooling bath was removed, the reaction was stirred at ambient temperature for 1 hour, quenched by adding excess saturated ammonium chloride, and partitioned between ether and brine. The organic layer was washed with saturated aqueous Na2S2O5, brine, dried (Na2SO4), filtered, and concentrated under vacuum. Purification on silica gel with hexanes gave the title compound (5.34 g, 79%) as a colorless oil.

後処理

  1. customthe cooling bath was removed
  2. stirringthe reaction was stirred 0.5 hours at ambient temperature
  3. customto give a dark red homogeneous solution which
  4. temperaturewas cooled to −23° C
  5. customThe cooling bath was removed
  6. stirringthe reaction was stirred at ambient temperature for 1 hour
  7. customquenched
  8. additionby adding excess saturated ammonium chloride
  9. custompartitioned between ether and brine
  10. washThe organic layer was washed with saturated aqueous Na2S2O5, brine
  11. dry with materialdried (Na2SO4)
  12. filtrationfiltered
  13. concentrationconcentrated under vacuum
  14. customPurification on silica gel with hexanes

出典と根拠

ORDレコード
ord-156aa50acb8d4a6ab5bdfdd0c739052b
出典データセット
uspto-grants-2001_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06284796B1

反応ノート

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