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Acetic Acid → (2-Methyl-1H-inden-3-yl)acetic acid

HRID 437317
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HRID 437317 반응식
[CH3:1][CH:2]1[CH2:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]1=O.C([CH2:14][C:15]([OH:17])=[O:16])#N.C(O)(=O)C.C([O-])(=O)C.[NH4+]>C1(C)C=CC=CC=1>[CH3:1][C:2]1[CH2:10][C:9]2[C:4]([C:3]=1[CH2:14][C:15]([OH:17])=[O:16])=[CH:5][CH:6]=[CH:7][CH:8]=2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 176Acetic AcidHCID 9740Cyanoacetic acidHCID 2492622-MethylindanoneHCID 517165Ammonium Acetate

생성물 1

HCID 14419403(2-Methyl-1H-inden-3-yl)acetic acid

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

2-Methylindanone (0.112 mole), cyanacetic acid (10.5 g., 0.123 mole), acetic acid (6.6 g.), and ammonium acetate (1.7 g.) in dry toluene (15.5 ml.) was refluxed with stirring for 21 hrs., as the liberated water was collected in a Dean Stark trap. The toluene was concentrated and the residue dissolved in 60 ml. of hot ethanol and 14 ml. of 2.2 N aqueous potassium hydroxide solution. 22 g. Of 85% KOH in 150 ml. of water was added and the mixture refluxed for 13 hr. under N2. The ethanol was removed under vacuum, 500 ml. water added, the aqueous solution washed well with ether and then boiled with charcoal. The aqueous filtrate was acidified to pH 2 with 50% hydrochloric acid, cooled and the precipitate of 2-methylinden-3-acetic acid was collected.

후처리

  1. custom, as the liberated water was collected in a Dean Stark trap
  2. concentrationThe toluene was concentrated
  3. dissolutionthe residue dissolved in 60 ml
  4. additionof water was added
  5. temperaturethe mixture refluxed for 13 hr
  6. customThe ethanol was removed under vacuum, 500 ml
  7. additionwater added
  8. washthe aqueous solution washed well with ether
  9. temperaturecooled
  10. customthe precipitate of 2-methylinden-3-acetic acid was collected

출처 및 근거

ORD 기록
ord-6a7ee9c64f9e463eaa42d63efb564ed9
출처 데이터셋
uspto-grants-1977_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04030994

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