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Stannous chloride dihydrate → 4-[(3-Methyl-1,2-benzisoxazol-4-yl)oxy]aniline

HRID 527515
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HRID 527515 반응식
[CH3:1][C:2]1[C:6]2[C:7]([O:11][C:12]3[CH:17]=[CH:16][C:15]([N+:18]([O-])=O)=[CH:14][CH:13]=3)=[CH:8][CH:9]=[CH:10][C:5]=2[O:4][N:3]=1.O.O.[Sn](Cl)Cl>CCO>[CH3:1][C:2]1[C:6]2[C:7]([O:11][C:12]3[CH:17]=[CH:16][C:15]([NH2:18])=[CH:14][CH:13]=3)=[CH:8][CH:9]=[CH:10][C:5]=2[O:4][N:3]=1
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참가 물질

4

반응물 2

HCID 61436Stannous chloride dihydrateHCID 679604203-Methyl-4-[(4-nitrophenyl)oxy]-1,2-benzisoxazole2회

생성물 1

HCID 679606614-[(3-Methyl-1,2-benzisoxazol-4-yl)oxy]aniline수율 33.7%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
90 °C

실험 절차

3-methyl-4-[(4-nitrophenyl)oxy]-1,2-benzisoxazole (Intermediate 11, 100 mg) was dissolved under nitrogen atmosphere in 5.0 ml of EtOH. Tin(II) chloride dihydrate (417 mg, 1.85 mmol) was added. The reaction mixture was then stirred at 90° C. for 5 hours. After removal of the volatiles, water was added and the reaction mixture was extracted two times with ethyl acetate. The collected organic layers were washed with a 5% aqueous solution of NaHCO3, dried over sodium sulphate, filtered and evaporated. The crude obtained was purified by a NH column and eluted with DCM/MeOH (100/0, then a gradient from 100/0 to 90/10, then 90/10) to afford 30 mg of the title compound.

후처리

  1. customAfter removal of the volatiles, water
  2. additionwas added
  3. extractionthe reaction mixture was extracted two times with ethyl acetate
  4. washThe collected organic layers were washed with a 5% aqueous solution of NaHCO3
  5. dry with materialdried over sodium sulphate
  6. filtrationfiltered
  7. customevaporated
  8. customThe crude obtained
  9. customwas purified by a NH column
  10. washeluted with DCM/MeOH (100/0

출처 및 근거

ORD 기록
ord-cb82aca0a4224a9bb8824a84d38dc547
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09346790B2

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