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

HRID 1246550

반응식

HRID 1246550 반응식
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

참가 물질

6

반응물 3

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

생성물 1

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

시약·촉매·용매 2

HCID 24014Cupric Chloride촉매HCID 8058Hexane용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-0cbaf1b30fa141aa8b11baa26f977eee
출처 데이터셋
uspto-grants-2006_10
특허 번호
US07125903B1

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