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

HRID 527515
ノート
印刷プレビュー

反応式

HRID 527515 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 61436Stannous chloride dihydrateHCID 679604203-Methyl-4-[(4-nitrophenyl)oxy]-1,2-benzisoxazole2 回

生成物 1

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

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
90 °C

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-cb82aca0a4224a9bb8824a84d38dc547
出典データセット
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09346790B2

反応ノート

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