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Nitromethane → 2-Bromo-1-cyclopropylmethoxy-3-(2-nitro-vinyl)-benzene

HRID 523996
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반응식

HRID 523996 반응식
[Br:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]([C:9]=1[O:10][CH2:11][CH:12]1[CH2:14][CH2:13]1)C=O.[N+:15]([CH3:18])([O-:17])=[O:16].[C:19]([O-])(=O)C.[NH4+]>CC(O)=O>[Br:1][C:2]1[C:3]([CH:19]=[CH:18][N+:15]([O-:17])=[O:16])=[CH:4][CH:5]=[CH:6][C:9]=1[O:10][CH2:11][CH:12]1[CH2:13][CH2:14]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6375NitromethaneHCID 517165Ammonium AcetateHCID 597250443-Bromo-2-(cyclopropylmethoxy)benzaldehyde

생성물 1

HCID 1317355752-Bromo-1-cyclopropylmethoxy-3-(2-nitro-vinyl)-benzene

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

380 mg (1.49 mmol) 5-Bromo-6-cyclopropylmethoxy-benzaldehyde (example XIX), 239 μL (4.47 mmol) nitromethane and 115 mg (1.49 mmol) ammonium acetate in 1.2 mL AcOH are stirred at 100° C. for 2 h. The reaction mixture is cooled to r.t. and quenched by the addition of 4 mL MeOH and 0.9 mL water. After stirring at r.t. for 1 h the precipitate is filtered off and dried at 40° C.

후처리

  1. customquenched by the addition of 4 mL MeOH and 0.9 mL water
  2. filtrationis filtered off
  3. customdried at 40° C.

출처 및 근거

ORD 기록
ord-b11a8b9952fd47b09167a0a3d0bede74
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09340510B2

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