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HCID 802799, 화합물 → 2-(4-Methylphenyl)-1,3-benzoxazol-5-amine

HRID 1896742
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HRID 1896742 반응식
[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
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참가 물질

4

반응물 1

HCID 802799HCID 802799, 화합물

생성물 1

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

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 22609514Ethyl acetate acetate용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-c55ae85c07ac4428b4719d374e16e254
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08518980B2

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