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

HRID 1956167
ノート
印刷プレビュー

反応式

HRID 1956167 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 86584057Phosphorus Pentoxide-Methanesulfonic Acid溶媒

反応条件

温度
50 °C

実験手順

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.

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート

後処理

  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

出典と根拠

ORDレコード
ord-ca2e048b9f4f4aaf988d50d10506568e
出典データセット
uspto-grants-1998_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05780465

反応ノート

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