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Nitroethane → HCID 2063266, 화합물

HRID 1873861
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HRID 1873861 반응식
[Cl:1][C:2]1[CH:9]=[C:8]([Cl:10])[CH:7]=[CH:6][C:3]=1[CH:4]=O.[N+:11]([CH2:14][CH3:15])([O-:13])=[O:12].C([O-])(=O)C.[NH4+]>C(O)(=O)C>[Cl:1][C:2]1[CH:9]=[C:8]([Cl:10])[CH:7]=[CH:6][C:3]=1/[CH:4]=[C:14](/[N+:11]([O-:13])=[O:12])\[CH3:15]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6587NitroethaneHCID 134042,4-DichlorobenzaldehydeHCID 517165Ammonium Acetate

생성물 1

HCID 2063266HCID 2063266, 화합물수율 55%

시약·촉매·용매 1

HCID 176Acetic Acid용매

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온도
90 °C

실험 절차

In a sulfonation flask 2,4-dichloro-benzaldehyde (77 g, 0.44 mol), nitroethane (216 ml, 3.04 mol) and ammonium acetate (81.4 g, 1.06 mol) were added to glacial acetic acid (600 ml). The resulting solution was heated to 90° C. for three hours. After removal of the solvent ice-water (400 ml) was added. The solid product was collected by filtration, washed with water and recrystallized from ethanol. 55.9 g (55% of theory) of 2,4-dichloro-1-((E)-2-nitro-propenyl)-benzene was obtained in the form of a yellow solid (m.p. 79-81° C.).

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  1. customAfter removal of the solvent ice-water (400 ml)
  2. additionwas added
  3. filtrationThe solid product was collected by filtration
  4. washwashed with water
  5. customrecrystallized from ethanol

출처 및 근거

ORD 기록
ord-54c3d0323e564db8b3057d7b3fb7aa5e
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08304444B2

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