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1,4-Dioxane → Phenanthrene-2-carboxylic acid

HRID 895375
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HRID 895375 반응식
Br[O-:2].[Na+].C([C:7]1[CH:20]=[CH:19][C:18]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[CH:11]=[CH:10][C:9]=2[CH:8]=1)(=O)C.[O:21]1[CH2:26]COCC1>>[C:26]([C:7]1[CH:20]=[CH:19][C:18]2[C:13]3[C:12](=[CH:17][CH:16]=[CH:15][CH:14]=3)[CH:11]=[CH:10][C:9]=2[CH:8]=1)([OH:21])=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 312751,4-DioxaneHCID 80060Methyl 2-phenanthryl ketoneHCID 23673712Sodium hypobromite

생성물 1

HCID 13234903Phenanthrene-2-carboxylic acid수율 99.2%

실험 절차

Bromine (4.7 ml, 0.091 mol) was added to an ice-cold solution of sodium hydroxide (12.7 g, 0.318 mol) in water (70 ml) to form a basic solution of sodium hypobromite. The sodium hypobromite solution was added to a stirred solution of 2-acetylphenanthrene in dioxane (70 ml) at 60-65 ° C. for 15 min. Excess sodium hypobromite was removed by the addition of 10% solution of sodium metabisulphite (20 ml). Water (300 ml) was added and approximately 100 ml of solvent was removed under reduced pressure. The reaction mixture was acidified with concentrated HCl. The precipitate formed was filtered and washed with water to give the title compound as a solid (4.01 g, 99.2%).

후처리

  1. customExcess sodium hypobromite was removed by the addition of 10% solution of sodium metabisulphite (20 ml)
  2. additionWater (300 ml) was added
  3. customapproximately 100 ml of solvent was removed under reduced pressure
  4. customThe precipitate formed
  5. filtrationwas filtered
  6. washwashed with water

출처 및 근거

ORD 기록
ord-f0f617a3bb174b52a4f0a992b1192dcf
출처 데이터셋
uspto-grants-2005_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06916816B2

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