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2-[4-(4-Nitrophenoxy)phenyl]oxazole → 4-[4-(2-Oxazolyl)phenoxy]benzenamine

HRID 630319
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인쇄 미리보기

반응식

HRID 630319 반응식
[N+:1]([C:4]1[CH:21]=[CH:20][C:7]([O:8][C:9]2[CH:14]=[CH:13][C:12]([C:15]3[O:16][CH:17]=[CH:18][N:19]=3)=[CH:11][CH:10]=2)=[CH:6][CH:5]=1)([O-])=O>C(OCC)(=O)C.CO.[Pd]>[O:16]1[CH:17]=[CH:18][N:19]=[C:15]1[C:12]1[CH:13]=[CH:14][C:9]([O:8][C:7]2[CH:20]=[CH:21][C:4]([NH2:1])=[CH:5][CH:6]=2)=[CH:10][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 684907472-[4-(4-Nitrophenoxy)phenyl]oxazole

생성물 1

HCID 684898744-[4-(2-Oxazolyl)phenoxy]benzenamine수율 103.4%

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 887Methanol용매HCID 8857Ethyl Acetate용매

실험 절차

A slurry of 2-[4-(4-nitrophenoxy)phenyl]oxazole (2.6 g, 9.2 mmol) in a mixture of ethyl acetate (20 mL) and methanol (100 mL) was placed under a nitrogen atmosphere before the addition of catalyst palladium (10% on C, 0.65 g). The reaction mixture was placed under a hydrogen atmosphere at atmospheric pressure. After 3 hours, the reaction mixture was filtered through a pad of Celite and washed with methanol. The filtrate was concentrated to give the 2.4 g of 4-[4-(2-oxazolyl)phenoxy]benzenamine.

후처리

  1. filtrationthe reaction mixture was filtered through a pad of Celite
  2. washwashed with methanol
  3. concentrationThe filtrate was concentrated

출처 및 근거

ORD 기록
ord-64f57226bd874fd4873ea72ec1a72f92
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09315509B2

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