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Diisobutylaluminumhydride → 2-(2-Bromo-4-fluorophenoxy)propionaldehyde

HRID 1824921
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HRID 1824921 반응식
[Br:1][C:2]1[CH:15]=[C:14]([F:16])[CH:13]=[CH:12][C:3]=1[O:4][CH:5]([CH3:11])[C:6](OCC)=[O:7].[H-].C([Al+]CC(C)C)C(C)C>C1(C)C=CC=CC=1>[Br:1][C:2]1[CH:15]=[C:14]([F:16])[CH:13]=[CH:12][C:3]=1[O:4][CH:5]([CH3:11])[CH:6]=[O:7]
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참가 물질

4

반응물 2

HCID 21225700DiisobutylaluminumhydrideHCID 22144730Ethyl 2-(2'-bromo-4'-fluorophenoxy)propionate

생성물 1

HCID 221447442-(2-Bromo-4-fluorophenoxy)propionaldehyde수율 102.6%

시약·촉매·용매 1

HCID 1140Toluene용매

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온도
-78 °C

실험 절차

A solution of 19.4 gm (66.7 mMol) ethyl 2-(2-bromo-4-fluorophenoxy)propionate in 400 mL toluene was cooled to −78° C. at which point 100 mL (100 mMol) diisobutylaluminum hydride (1 M in toluene) were added dropwise over 35 minutes. The reaction mixture was stirred at −78° C. for an additional 20 minutes after the addition was complete and then the reaction was quenched by the addition of methanol. The reaction mixture was warmed to room temperature and then treated with saturated aqueous sodium potassium carbonate. The mixture was stirred for 30 minutes and was then extracted well with ethyl acetate. The organic phases were combined, dried over sodium sulfate, and concentrated under reduced pressure to provide 16.9 gm of crude desired compound.

후처리

  1. additionwere added dropwise over 35 minutes
  2. additionafter the addition
  3. customthe reaction was quenched by the addition of methanol
  4. temperatureThe reaction mixture was warmed to room temperature
  5. additiontreated with saturated aqueous sodium potassium carbonate
  6. stirringThe mixture was stirred for 30 minutes
  7. extractionwas then extracted well with ethyl acetate
  8. dry with materialdried over sodium sulfate
  9. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-40821cd678f541069ddefc36a62680fe
출처 데이터셋
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07045545B1

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