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Water → 6-Ethyl-2,3-dihydro-1H-inden-1-one

HRID 1956167
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HRID 1956167 반응식
[CH2:1]([C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH2:10][C:11]([OH:13])=O)=[CH:5][CH:4]=1)[CH3:2].O>CS(O)(=O)=O.O=P12OP3(OP(OP(O3)(O1)=O)(=O)O2)=O>[CH2:1]([C:3]1[CH:4]=[C:5]2[C:6]([CH2:9][CH2:10][C:11]2=[O:13])=[CH:7][CH:8]=1)[CH3:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 962WaterHCID 20640393-(4-ethylphenyl)propanoic Acid

생성물 1

HCID 223634256-Ethyl-2,3-dihydro-1H-inden-1-one

시약·촉매·용매 1

HCID 86584057Phosphorus Pentoxide-Methanesulfonic Acid용매

반응 조건

온도
50 °C

실험 절차

A 13.0 g sample of 3-(4-ethylphenyl)propanoic acid was dissolved in 125 g of Eaton's reagent and the mixture was heated at 50° C. with stirring for 3 hours. The resulting mixture was cooled and poured into water. The mixture obtained was extracted with ethyl acetate and the organic extract was dried over sodium sulfate and concentrated by evaporation under reduced pressure. The residue was distilled and the 7.8 g colorless liquid fraction boiling at 95°-100° C. under 0.5 mm Hg (66 Pascals) pressure was collected to obtain 6-ethyl-1-indanone.

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후처리

  1. temperatureThe resulting mixture was cooled
  2. customThe mixture obtained
  3. extractionwas extracted with ethyl acetate
  4. extractionthe organic extract
  5. dry with materialwas dried over sodium sulfate
  6. concentrationconcentrated by evaporation under reduced pressure
  7. distillationThe residue was distilled
  8. customthe 7.8 g colorless liquid fraction boiling at 95°-100° C. under 0.5 mm Hg (66 Pascals) pressure was collected

출처 및 근거

ORD 기록
ord-ca2e048b9f4f4aaf988d50d10506568e
출처 데이터셋
uspto-grants-1998_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05780465

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