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4-Nitrobenzaldehyde → HCID 178498134, 화합물

HRID 1801284
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HRID 1801284 반응식
[NH2:1][C:2]1[CH:11]=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[CH:4][CH:3]=1.[N+:12]([C:15]1[CH:22]=[CH:21][C:18]([CH:19]=O)=[CH:17][CH:16]=1)([O-:14])=[O:13]>C(O)C>[N+:12]([C:15]1[CH:22]=[CH:21][C:18](/[CH:19]=[N:1]/[C:2]2[CH:3]=[CH:4][C:5]([C:6]([O:8][CH3:9])=[O:7])=[CH:10][CH:11]=2)=[CH:17][CH:16]=1)([O-:14])=[O:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 5414-NitrobenzaldehydeHCID 12082Methyl 4-aminobenzoate

생성물 1

HCID 178498134HCID 178498134, 화합물수율 103.1%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of methyl 4-aminobenzoate (1.51 g, 10 mmol) and 4-nitrobenzaldehyde (1.51 g, 10 mmol) in ethanol (30 mL) was stirred overnight to give the yellow slurry. The precipitated off-white solid was collected and dried in vacuo to give (E)-methyl 4-(4-nitrobenzylideneamino)benzoate (2.93 g, 95% yield).

후처리

  1. customto give the yellow slurry
  2. customThe precipitated off-white solid was collected
  3. customdried in vacuo

출처 및 근거

ORD 기록
ord-1ae6f3957d4647b9b2551f960ebad5ea
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08344137B2

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