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4-Chlorobenzaldehyde → HCID 54040399, 화합물

HRID 2253747
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HRID 2253747 반응식
[Br-].C1([PH+](C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[Li]CCCC.[Cl:26][C:27]1[CH:34]=[CH:33][C:30]([CH:31]=O)=[CH:29][CH:28]=1.[CH2:35]1C[O:38][CH2:37][CH2:36]1>>[Cl:26][C:27]1[CH:34]=[CH:33][C:30]([CH:31]=[CH:35][CH2:36][CH2:37][OH:38])=[CH:29][CH:28]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 77264-ChlorobenzaldehydeHCID 8028TetrahydrofuranHCID 517696Phosphine, triphenyl-, hydrobromideHCID 178418339Butyllithium

생성물 1

HCID 54040399HCID 54040399, 화합물

실험 절차

To a suspension of 3-((2-methoxy)-2-propoxy)propyl)triphenyl phosphonium bromide (4.42 g, 10 mmoles) in THF (100 mL) was added n-BuLi (6 mL of 1.6M) at -78°. The reaction mixture was stirred at -78° for 30 min. 4-Chlorobenzaldehyde (1.4 g, 10 mM) was added and the reaction was warmed to RT. The reaction mixture was quenched with buffer and extracted with ethyl acetate. After evaporation of the ethyl acetate, the crude residue was dissolved in 25 mL THF and 5 mL of AcOH plus 5 mL H2O was added. The mixture was stirred for 2 hours at RT and evaporated. The residue was extracted with ethyl acetate, and the ethyl acetate evaporated. Flash chromatography of the residue using 25% ethyl acetate/hexane afforded the title compound as a mixture of cis and trans isomers.

후처리

  1. customThe reaction mixture was quenched with buffer and
  2. extractionextracted with ethyl acetate
  3. customAfter evaporation of the ethyl acetate
  4. dissolutionthe crude residue was dissolved in 25 mL THF
  5. addition5 mL of AcOH plus 5 mL H2O was added
  6. stirringThe mixture was stirred for 2 hours at RT
  7. customevaporated
  8. extractionThe residue was extracted with ethyl acetate
  9. customthe ethyl acetate evaporated

출처 및 근거

ORD 기록
ord-6692d713f4404ed9a96fbf3b7c22552f
출처 데이터셋
uspto-grants-1993_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05232916

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