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N-bromobutanimide → 2'-Bromomethyl-biphenyl-4-carboxylic acid ethyl ester

HRID 719730
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HRID 719730 반응식
C(OC(C1C=C(C2C=CC(C[Br:19])=CC=2)C=CC=1)=O)C.[CH2:20]([O:22][C:23]([C:25]1[CH:30]=[CH:29][C:28]([C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][C:32]=2[CH3:37])=[CH:27][CH:26]=1)=[O:24])[CH3:21].BrN1C(=O)CCC1=O>C(Cl)(Cl)(Cl)Cl.N(C(C)(C)C#N)=NC(C)(C)C#N>[CH2:20]([O:22][C:23]([C:25]1[CH:30]=[CH:29][C:28]([C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][C:32]=2[CH2:37][Br:19])=[CH:27][CH:26]=1)=[O:24])[CH3:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 67184N-bromobutanimideHCID 121718932'-Methylbiphenyl-4-carboxylic acid ethyl esterHCID 214642554'-Bromomethyl-biphenyl-3-carboxylic acid ethyl ester

생성물 1

HCID 219992402'-Bromomethyl-biphenyl-4-carboxylic acid ethyl ester수율 99%

시약·촉매·용매 2

HCID 6547Azobisisobutyronitrile촉매
HCID 5943
Carbon Tetrachloride
용매

실험 절차

2′-Bromomethyl-biphenyl4-carboxylic acid ethyl ester was synthesized as described for 4′-bromomethyl-biphenyl-3-carboxylic acid ethyl ester. 2′-Methyl-biphenyl-4-carboxylic acid ethyl ester (4.4 g, 18.31 mmol, 1 eq.) in carbon tetrachloride was treated with N-bromosuccinimide (3.58 g, 20.14 mmol, 1.1 eq.), and 2,2′-azobisisobutyronitrile (0.15 g, 0.92 mmol, 5 mol %). When complete, the reaction was worked up as described leaving 2′-bromomethyl-biphenyl-4-carboxylic acid ethyl ester (5.77 g, 99% yield) as a yellow oil.

후처리

  1. custom2′-Bromomethyl-biphenyl4-carboxylic acid ethyl ester was synthesized

출처 및 근거

ORD 기록
ord-41d7aa59ad0945c0afdc1468984c3bc6
출처 데이터셋
uspto-grants-2006_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07132456B2

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