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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → 3-Formylbut-2-enyl acetate

HRID 260568
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HRID 260568 반응식
[C:1]([O:4][CH2:5][CH:6]=[C:7]([CH3:10])[CH2:8][OH:9])(=[O:3])[CH3:2].O>CN(C)C=O>[C:1]([O:4][CH2:5][CH:6]=[C:7]([CH3:10])[CH:8]=[O:9])(=[O:3])[CH3:2]
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참가 물질

4

반응물 2

HCID 962WaterHCID 5382224-Acetoxy-2-methyl-2-buten-1-ol

생성물 1

HCID 846993-Formylbut-2-enyl acetate수율 91.2%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a solution of 4-acetoxy-2-methyl-2-buten-1-ol (6.69 g, 46.4 mmol) in dimethylformamide (40 ml) were added 2,2,6,6-tetramethyl-piperidine-1-oxy (0.39 g, 2.32 mmol, 5 mol %) and cuprous chloride (0.48 g, 4.64 mmol, 10 mol %). The mixture was subjected to reaction at 40° C. for 8 hours while bubbling oxygen at a rate of about 100 ml/min. After completion of the reaction, the reaction mixture was poured into ice-cooled water (30 ml) and extracted with ether (100 ml) three times. The extract was dried over anhydrous magnesium sulfate. Evaporation of the ether followed by purification by column chromatography (ethyl acetate-hexane (=1:3)) gave 4-acetoxy-2-methyl-2-buten-1-al (6.02 g, 42.3 mmol; Yield: 91.2%).

후처리

  1. customThe mixture was subjected to reaction at 40° C. for 8 hours
  2. customwhile bubbling oxygen at a rate of about 100 ml/min
  3. customAfter completion of the reaction
  4. additionthe reaction mixture was poured into ice-
  5. extractionextracted with ether (100 ml) three times
  6. dry with materialThe extract was dried over anhydrous magnesium sulfate
  7. customEvaporation of the ether
  8. customfollowed by purification by column chromatography (ethyl acetate-hexane (=1:3))

출처 및 근거

ORD 기록
ord-81e0ab3abfbe4e8fbf8e7f4e5262a06e
출처 데이터셋
uspto-grants-1996_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05527952

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