Sulfuric Acid → HCID 11572310, 화합물

HRID 223122노트

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HRID 223122 반응식
[CH:1]([CH:4]1[C:12]2[C:7](=[CH:8][C:9]([CH3:15])=[C:10]([Mg]Br)[CH:11]=2)[C:6]([CH3:17])([CH3:16])[CH:5]1[CH3:18])([CH3:3])[CH3:2].[Mg].BrC1C=C2C(C(C)(C)C(C)C2C(C)C)=CC=1C.S(=O)(=O)(O)O.CN(C)[CH:44]=[O:45]>>[CH:44]([C:10]1[CH:11]=[C:12]2[C:7]([C:6]([CH3:17])([CH3:16])[CH:5]([CH3:18])[CH:4]2[CH:1]([CH3:3])[CH3:2])=[CH:8][C:9]=1[CH3:15])=[O:45]

참가 물질

6

실험 절차

40 ml Bromine is added at 10° C. to a solution of 100 g 1-isopropyl-2,3,3,5-tetramethyl indan (obtained according to Example I or II) and 1 ml pyridine in 50 ml carbon tetrachloride. Then the reaction mixture is stirred during one hour and poured out into an aqueous solution of approximately 25 g sodium thiosulphate. The organic layer is separated, washed with 25% sodium hydroxide and evaporated. The residue is distilled under diminished pressure yielding 105 g 6-bromo-1-isopropyl-2,3,3,5-tetramethyl indan. B.p. 145°-150° C./1 mm Hg. 25 g Dimethyl formamide is added to a solution of 1-isopropyl-2,3,3,5-tetramethyl-6-indanyl magnesium bromide, prepared from 9 g magnesium and 100 g of the 6-bromo indan obtained above. The reaction mixture is then heated to reflux during 30 min., poured out into a mixture of ice and diluted sulphuric acid and extracted with ether. The solution in ether is washed neutral, dried and evaporated. The residue is distilled under diminished pressure yielding 30 g 6-formyl-1-isopropyl-2,3,3,5-tetramethyl indan. B.p. 135° C./1 mm Hg.

후처리

  1. customobtained above
  2. temperatureThe reaction mixture is then heated
  3. temperatureto reflux during 30 min.
  4. extractionextracted with ether
  5. washThe solution in ether is washed neutral
  6. customdried
  7. customevaporated
  8. distillationThe residue is distilled under diminished pressure

출처 및 근거

ORD 기록
ord-34a1c3a1232e4669b93460c7e1369b2a
출처 데이터셋
uspto-grants-1982_10
특허 번호
US04352748

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