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2-Methyl-5-(2-methyl-4-nitrophenoxy)benzo[d]oxazole → 3-Methyl-4-(2-methylbenzo[d]oxazol-5-yloxy)benzenamine

HRID 240541
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인쇄 미리보기

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HRID 240541 반응식
[CH3:1][C:2]1[O:3][C:4]2[CH:10]=[CH:9][C:8]([O:11][C:12]3[CH:17]=[CH:16][C:15]([N+:18]([O-])=O)=[CH:14][C:13]=3[CH3:21])=[CH:7][C:5]=2[N:6]=1.[H][H]>C(O)C.[Pd]>[CH3:21][C:13]1[CH:14]=[C:15]([NH2:18])[CH:16]=[CH:17][C:12]=1[O:11][C:8]1[CH:9]=[CH:10][C:4]2[O:3][C:2]([CH3:1])=[N:6][C:5]=2[CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 669369092-Methyl-5-(2-methyl-4-nitrophenoxy)benzo[d]oxazoleHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 669372733-Methyl-4-(2-methylbenzo[d]oxazol-5-yloxy)benzenamine수율 69%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

To a solution of 2-methyl-5-(2-methyl-4-nitrophenoxy)benzo[d]oxazole (671 mg, 2.36 mmol) in ethanol (10 mL) was added 10% palladium on carbon (50 mg, 0.047 mmol). The reaction mixture was subjected to 40 psi of hydrogen for 2.5 hours. The mixture was filtered and the filtrate was concentrated under reduced pressure. The residue was chromatographed to provide the product (0.411 g, 69%) as yellow oil.

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후처리

  1. filtrationThe mixture was filtered
  2. concentrationthe filtrate was concentrated under reduced pressure
  3. customThe residue was chromatographed

출처 및 근거

ORD 기록
ord-ddbadea473d84e6d97d92ef8dd4792ee
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08648087B2

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