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Methoxymethyl-triphenylphosphonium chloride → 1-bromo-2-(methyloxy)-3-[(E)-2-(methyloxy)ethenyl]benzene

HRID 1942669
ノート
印刷プレビュー

反応式

HRID 1942669 の反応式
[Cl-].[CH3:2][O:3][CH2:4][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.[Li]CCCC.[Br:29][C:30]1[C:31]([O:38][CH3:39])=[C:32]([CH:35]=[CH:36][CH:37]=1)[CH:33]=O>C1COCC1>[Br:29][C:30]1[CH:37]=[CH:36][CH:35]=[C:32](/[CH:33]=[CH:2]/[O:3][CH3:4])[C:31]=1[O:38][CH3:39]
参加物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 2723798Methoxymethyl-triphenylphosphonium chlorideHCID 110638083-Bromo-2-methoxybenzaldehydeHCID 178418339Butyllithium

生成物 1

HCID 584941231-bromo-2-(methyloxy)-3-[(E)-2-(methyloxy)ethenyl]benzene収率 84.3%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

In a dried three-necked flask, to a solution of [(methyloxy)methyl](triphenyl) phosphonium chloride (3.59 g, 10.46 mmol) in THF (20 mL) was added BuLi (3.91 mL, 9.77 mmol) dropwise at −78° C. After addition, the reaction mixture was stirred at room temperature for 20 min. Then the reaction mixture was cooled to −78° C. A solution of 3-bromo-2-(methyloxy)benzaldehyde (D99) (1.5 g, 6.98 mmol) in THF (5 mL) to the reaction mixture dropwise. After addition, the reaction mixture was stirred at −78° C. for 2 hour and then warmed to room temperature. The mixture was stirred at room temperature overnight. Then the reaction was quenched with water. The organic phase was separated. The aqueous phase was extracted with EA (10 mL). The combined organic solution was dried over anhydrous sodium sulphate. After filtration, and concentration, the residue was purified by column chromatography (EA/Hexane: 0 to 30%) to give 1-bromo-2-(methyloxy)-3-[(E)-2-(methyloxy)ethenyl]benzene (D100) (1.43 g). MS (ES): C10H11BrO2 requires 241.9. found 243.0 (M+H+).

後処理

  1. additionAfter addition
  2. temperatureThen the reaction mixture was cooled to −78° C
  3. additionAfter addition
  4. stirringthe reaction mixture was stirred at −78° C. for 2 hour
  5. temperaturewarmed to room temperature
  6. stirringThe mixture was stirred at room temperature overnight
  7. customThen the reaction was quenched with water
  8. customThe organic phase was separated
  9. extractionThe aqueous phase was extracted with EA (10 mL)
  10. dry with materialThe combined organic solution was dried over anhydrous sodium sulphate
  11. filtrationAfter filtration, and concentration
  12. customthe residue was purified by column chromatography (EA/Hexane: 0 to 30%)

出典と根拠

ORDレコード
ord-9ce9bcb8ac0d4477a83bf425ded4758c
出典データセット
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08389508B2

反応ノート

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