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Potassium sodium tartarate → 2-(2-Hydroxyethyl)-2,3-dihydro-1H-inden-1-ol

HRID 1731148
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HRID 1731148 반응식
C([O:3][C:4](=O)[CH2:5][CH:6]1[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[C:7]1=[O:15])C.[H-].[Al+3].[Li+].[H-].[H-].[H-].C(C(C(C([O-])=O)O)O)([O-])=O.[K+].[Na+]>C1COCC1>[OH:15][CH:7]1[C:8]2[C:13](=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH2:14][CH:6]1[CH2:5][CH2:4][OH:3]
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참가 물질

5

반응물 3

HCID 9855836Potassium sodium tartarateHCID 111835591H-Indene-2-acetic acid, 2,3-dihydro-1-oxo-, ethyl esterHCID 21226445Aluminium lithium hydride

생성물 1

HCID 214953232-(2-Hydroxyethyl)-2,3-dihydro-1H-inden-1-ol

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A solution of 1-oxoindane-2-acetic acid ethyl ester acid (5 g), described in Example 475, in dry THF (20 ml) is added to a stirred slurry of lithium aluminum hydride (3.6 g) in 120 ml of the same solvent. The reaction mixture is heated at reflux for 36 hr., allowed to cool, and decomposed with 30% aqueous solution of sodium potassium tartrate (14.4 ml). After filtration, the precipitate is washed with THF. The filtrate and washing are dried. Removal of solvent gives an oil which crystallizes from benzene to give the title compound m.p. 80°-82° C.

후처리

  1. temperatureThe reaction mixture is heated
  2. temperatureat reflux for 36 hr
  3. temperatureto cool
  4. filtrationAfter filtration
  5. washthe precipitate is washed with THF
  6. washThe filtrate and washing
  7. customare dried
  8. customRemoval of solvent
  9. customgives an oil which
  10. customcrystallizes from benzene

출처 및 근거

ORD 기록
ord-64db10d8d98047ad869a670b152e2491
출처 데이터셋
uspto-grants-1976_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03995052

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