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Azobisisobutyronitrile → 5-(Bromomethyl)-2-pentyl-4-phenyl-1,3-oxazole

HRID 1982438
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HRID 1982438 반응식
[CH3:1][C:2]1[O:6][C:5]([CH2:7][CH2:8][CH2:9][CH2:10][CH3:11])=[N:4][C:3]=1[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.[Br:18]N1C(=O)CCC1=O.N(C(C)(C)C#N)=NC(C)(C)C#N>C(Cl)(Cl)(Cl)Cl>[Br:18][CH2:1][C:2]1[O:6][C:5]([CH2:7][CH2:8][CH2:9][CH2:10][CH3:11])=[N:4][C:3]=1[C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6547AzobisisobutyronitrileHCID 67184N-bromobutanimideHCID 233165955-Methyl-2-pentyl-4-phenyl-1,3-oxazole

생성물 1

HCID 233165985-(Bromomethyl)-2-pentyl-4-phenyl-1,3-oxazole

시약·촉매·용매 1

HCID 5943Carbon Tetrachloride용매

실험 절차

5-Methyl-2-pentyl-4-phenyloxazole (4.25 g) was brominated with N-bromosuccinimide (3.4 g) in carbon tetrachloride in the presence of azobisisobutyronitrile (0.2 g). The procedure gave an oil of 5-bromomethyl-2-pentyl-4-phenyloxazole, yield 5.70 g (99.7%).

출처 및 근거

ORD 기록
ord-bc81d66a0b11446d86671eebde14d4a8
출처 데이터셋
uspto-grants-1986_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04596816

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