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N-bromobutanimide → Ethyl 2-bromomethyl-3,4-dichlorobenzoate

HRID 1492391
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인쇄 미리보기

반응식

HRID 1492391 반응식
[Cl:1][C:2]1[C:3]([CH3:14])=[C:4]([CH:10]=[CH:11][C:12]=1[Cl:13])[C:5]([O:7][CH2:8][CH3:9])=[O:6].[Br:15]N1C(=O)CCC1=O>C(Cl)(Cl)(Cl)Cl>[Br:15][CH2:14][C:3]1[C:2]([Cl:1])=[C:12]([Cl:13])[CH:11]=[CH:10][C:4]=1[C:5]([O:7][CH2:8][CH3:9])=[O:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 67184N-bromobutanimideHCID 18950271HCID 18950271, 화합물

생성물 1

HCID 18950258Ethyl 2-bromomethyl-3,4-dichlorobenzoate수율 112.1%

시약·촉매·용매 1

HCID 5943Carbon Tetrachloride용매

실험 절차

A mixture of ethyl 3,4-dichloro-2-methylbenzoate (34.0 g), N-bromosuccinimide (30.0 g) and carbon tetrachloride was irradiated with u.v. light in a photochemical reactor for 3 hours. The cooled mixture was filtered and the filtrate washed with water, dried (magnesium sulphate) and evaporated to give ethyl 2-bromomethyl-3,4-dichlorobenzoate (51.0 g) as an oil, NMR (CDCl3) 1.45 (t,3H), 4.4 (q,2H), 5.15 (s,2H), 7.7 (m,2H).

후처리

  1. customwas irradiated with u.v
  2. filtrationThe cooled mixture was filtered
  3. washthe filtrate washed with water
  4. dry with materialdried (magnesium sulphate)
  5. customevaporated

출처 및 근거

ORD 기록
ord-22b70368b67a437b86e0a225731c07ce
출처 데이터셋
uspto-grants-1994_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05374606

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