Glycol monoethyl ether → 3-(3-Methoxyphenyl)thieno[2,3-d]isoxazole

HRID 1246550

反応式

HRID 1246550 の反応式
Br[C:2]1[CH:6]=[CH:5][S:4][C:3]=1[C:7]([C:10]1[CH:15]=[CH:14][CH:13]=[C:12]([O:16][CH3:17])[CH:11]=1)=[N:8][OH:9].[OH-].[K+].C(OCCO)C>[Cu](Cl)Cl.CCCCCC>[CH3:17][O:16][C:12]1[CH:11]=[C:10]([C:7]2[C:3]3[S:4][CH:5]=[CH:6][C:2]=3[O:9][N:8]=2)[CH:15]=[CH:14][CH:13]=1

参加物

6

反応物 3

HCID 8076Glycol monoethyl etherHCID 14797Potassium HydroxideHCID 72727313(3-Bromothien-2-yl) (3-methoxyphenyl)methanone oxime

生成物 1

HCID 140972413-(3-Methoxyphenyl)thieno[2,3-d]isoxazole収率 68%

試薬・触媒・溶媒 2

HCID 24014Cupric Chloride触媒HCID 8058Hexane溶媒

実験手順

Reflux a mixture of (3-bromothiophen-2-yl)-(3-methoxyphenyl)methanone oxime (10 g, 0.032 mol), KOH (3.6 g, 0.064 mol dissolved in 10 mL water) and 2-ethoxyethanol (100 mL) under nitrogen for one hour at 105–110° C. Add copper chloride (0.16 g, 0.0016 mol) whereupon the reaction mixture becomes dark brown in color. Heat the reaction for an additional one hour. Add water and extract the organics into ether. Wash the ether phase with water, dry (MgSO4), filter and concentrate to yield an oil. Purify the oil by column (alumina) chromatography, and elute with 15% ether in hexane to obtain white crystals. Recrystallize the crystals from ether:hexane to yield the title compound (5 g, 68% Yield), m.p. 51–52° C.

後処理

  1. temperatureReflux
  2. temperatureHeat
  3. customthe reaction for an additional one hour
  4. extractionAdd water and extract the organics into ether
  5. washWash the ether phase with water
  6. dry with materialdry (MgSO4)
  7. filtrationfilter
  8. concentrationconcentrate
  9. customto yield an oil
  10. customPurify the oil by column (alumina) chromatography
  11. washelute with 15% ether in hexane
  12. customto obtain white crystals
  13. customRecrystallize the crystals from ether

出典と根拠

ORDレコード
ord-0cbaf1b30fa141aa8b11baa26f977eee
出典データセット
uspto-grants-2006_10
特許番号
US07125903B1

関連ノート

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