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Ammonia → 3-Chloro-4,4-dimethylpent-2-enal

HRID 2408957
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HRID 2408957 반응식
P(Cl)(Cl)([Cl:3])=O.CN([CH:9]=[O:10])C.[CH3:11][C:12](=O)[C:13]([CH3:16])([CH3:15])[CH3:14].N>>[Cl:3][C:12]([C:13]([CH3:16])([CH3:15])[CH3:14])=[CH:11][CH:9]=[O:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 222AmmoniaHCID 6228DimethylformamideHCID 6416PinacoloneHCID 24813Phosphorus oxychloride

생성물 1

HCID 540583463-Chloro-4,4-dimethylpent-2-enal수율 80%

실험 절차

Phosphorous oxychloride (18.77 mL, 200 mmol) was added dropwise to DMF (30.8 mL, 400 mmol) at 0-5° C. for 30 min. Pinacolone (10 g, 100 mmol) was added dropwise to the reaction mixture at the same temperature for 30 min. The mixture was allowed to rt and stirred for 2 h. The reaction mixture was poured into ice cold water and basified with ammonia solution. The solution was extracted with chloroform (3×200 mL) and the combined chloroform layer was washed with water, brine and dried over sodium sulfate. The solution was filtered and evaporated the solvent. The residue was chromatographed over silica gel column using hexane-EtoAc (97:3) as eluents to give the product as a pale green color oil (11.7 g, 80%).

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후처리

  1. customwas allowed to rt
  2. additionThe reaction mixture was poured into ice cold water
  3. extractionThe solution was extracted with chloroform (3×200 mL)
  4. washthe combined chloroform layer was washed with water, brine
  5. dry with materialdried over sodium sulfate
  6. filtrationThe solution was filtered
  7. customevaporated the solvent
  8. customThe residue was chromatographed over silica gel column

출처 및 근거

ORD 기록
ord-465de8153cb54704af761d8296558125
출처 데이터셋
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08815879B2

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