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Allyl Alcohol → 3-(4-Acetamidophenyl)propanal

HRID 1242263
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HRID 1242263 반응식
I[C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:9](=[O:11])[CH3:10])=[CH:4][CH:3]=1.C([O-])(O)=O.[Na+].[CH2:17]([OH:20])[CH:18]=[CH2:19]>[Cl-].C([N+](CCCC)(CCCC)CCCC)CCC.Cl[Pd]Cl.CN(C=O)C>[C:9]([NH:8][C:5]1[CH:6]=[CH:7][C:2]([CH2:19][CH2:18][CH:17]=[O:20])=[CH:3][CH:4]=1)(=[O:11])[CH3:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 7858Allyl AlcoholHCID 12147N-(4-Iodophenyl)acetamideHCID 516892Sodium Bicarbonate

생성물 1

HCID 99206073-(4-Acetamidophenyl)propanal수율 23.9%

시약·촉매·용매 3

HCID 24290Palladium Chloride촉매HCID 70681Tetrabutylammonium Chloride
촉매
HCID 6228Dimethylformamide용매

실험 절차

To a mixture of N-(4-Iodophenyl)acetamide (10.8 g, 42 mmol, 1.0 equiv) and DMF (50.0 ml) were added tetrabutylammonium chloride (11.7 g, 42 mmol, 1.0 equiv), NaHCO3 (8.7 g, 105 mmol), and allyl alcohol (4.2 ml, 63 mmol, 1.5 equiv) and the mixture was stirred for 10 min. To the resulting mixture PdCl2 (1.21 g, 9.6 mmol, 0.23 equiv) was added and the mixture was stirred under nitrogen for 45 h. The resulting mixture was extracted with EtOAc (3×100 ml). The combined extracts were washed with 5% HCl, brine, dried over MgSO4 and concentrated under vacuum. The residue was purified by column chromatography (EtOAc:hexane 70:30) to give 3-(4′-Acetamidophenyl)-1-propanal (1.92 g, 23.1%) which was used as such in the next step.

후처리

  1. stirringthe mixture was stirred under nitrogen for 45 h
  2. extractionThe resulting mixture was extracted with EtOAc (3×100 ml)
  3. washThe combined extracts were washed with 5% HCl, brine
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated under vacuum
  6. customThe residue was purified by column chromatography (EtOAc:hexane 70:30)

출처 및 근거

ORD 기록
ord-e41e43ed183141d2bfe6d5f6ae3ede99
출처 데이터셋
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07115666B2

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