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Hydrogen Peroxide → HCID 21543589, 화합물

HRID 1606586
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HRID 1606586 반응식
[O:1]=[C:2]1[C:14]2[CH:13]=[C:12]([C:15]([OH:17])=[O:16])[CH:11]=[CH:10][C:9]=2[C:8]2[C:3]1=[CH:4][C:5]([C:18]([OH:20])=[O:19])=[CH:6][CH:7]=2.[OH:21]O>S(=O)(=O)(O)O>[O:21]=[C:2]1[O:1][C:14]2[CH:13]=[C:12]([C:15]([OH:17])=[O:16])[CH:11]=[CH:10][C:9]=2[C:8]2[CH:7]=[CH:6][C:5]([C:18]([OH:20])=[O:19])=[CH:4][C:3]1=2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 784Hydrogen PeroxideHCID 27589459-Oxo-9H-fluorene-2,7-dicarboxylic acid

생성물 1

HCID 21543589HCID 21543589, 화합물

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

실험 절차

A suspension of 12.0 g (0.045 mole) of 9-oxo-fluorene-2,7-dicarboxylic acid in 100 ml of concentrated sulfuric acid is slowly reacted with 12.0 ml of a 30% hydrogen peroxide solution. The reaction is strongly exothermic and is controlled by cooling the stirred reaction mixture in a water bath. The cooled reaction mixture is poured onto 500 ml of an ice water mixture, filtered and washed with water. The residue is resuspended in water, stirred, filtered and washed with a total of about 350 ml of deionized water, to yield 11.2 g of 6-oxo-6H-dibenzo[b,d] pyran-3,8-dicarboxylic acid having a m.p. greater than 300° C. EXAMPLE IV

후처리

  1. temperatureby cooling
  2. customthe stirred reaction mixture in a water bath
  3. customThe cooled reaction mixture
  4. filtrationfiltered
  5. washwashed with water
  6. filtrationfiltered
  7. washwashed with a total of about 350 ml of deionized water

출처 및 근거

ORD 기록
ord-0d2ff226ff144cf089d101990a9ab839
출처 데이터셋
uspto-grants-1976_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03953455

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