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HCID 802799、化合物 → 2-(4-Methylphenyl)-1,3-benzoxazol-5-amine

HRID 1886910
ノート
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反応式

HRID 1886910 の反応式
[N+:1]([C:4]1[CH:5]=[CH:6][C:7]2[O:11][C:10]([C:12]3[CH:17]=[CH:16][C:15]([CH3:18])=[CH:14][CH:13]=3)=[N:9][C:8]=2[CH:19]=1)([O-])=O>C(OCC)(=O)C.C(O)(=O)C.[Pd]>[C:15]1([CH3:18])[CH:14]=[CH:13][C:12]([C:10]2[O:11][C:7]3[CH:6]=[CH:5][C:4]([NH2:1])=[CH:19][C:8]=3[N:9]=2)=[CH:17][CH:16]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

HCID 802799HCID 802799、化合物

生成物 1

HCID 7218792-(4-Methylphenyl)-1,3-benzoxazol-5-amine収率 60%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 22609514Ethyl acetate acetate溶媒

実験手順

To 5-nitro-2-p-tolylbenzo[d]oxazole (4.8 g, 18.90 mmol) in ethyl acetate/acetic acid (250 ml/1 mL) was added palladium on carbon (480 mg). The reaction vessel was purged three times with nitrogen, followed by hydrogen three times, and then left stirring under hydrogen for 16 h. The reaction vessel was finally purged three times with nitrogen, before filtration on a pad of Celite®, which was washed with ethyl acetate. The organic solution was washed with saturated aqueous Na2CO3, followed by brine. The combined organic layers were dried over anhydrous MgSO4 and evaporated to afford 2.5 g (60%) of the title compound.

後処理

  1. customThe reaction vessel was purged three times with nitrogen
  2. waitleft
  3. customThe reaction vessel was finally purged three times with nitrogen
  4. filtrationbefore filtration on a pad of Celite®, which
  5. washwas washed with ethyl acetate
  6. washThe organic solution was washed with saturated aqueous Na2CO3
  7. dry with materialThe combined organic layers were dried over anhydrous MgSO4
  8. customevaporated

出典と根拠

ORDレコード
ord-1dcbd6b8cd0d4e1d8711f350d054b1b2
出典データセット
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08501713B2

反応ノート

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