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Sulfuric Acid → 4-Ethynyl-3-nitrosobenzamide

HRID 1844790
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HRID 1844790 반응식
[C:1]([C:3]1[CH:11]=[CH:10][C:6]([C:7]([NH2:9])=[O:8])=[CH:5][C:4]=1[NH2:12])#[CH:2].S(=O)(=O)(O)[OH:14].[Cr](O[Cr]([O-])(=O)=O)([O-])(=O)=O.[K+].[K+]>O>[C:1]([C:3]1[CH:11]=[CH:10][C:6]([C:7]([NH2:9])=[O:8])=[CH:5][C:4]=1[N:12]=[O:14])#[CH:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1118Sulfuric AcidHCID 24502Potassium DichromateHCID 866947874-Ethynyl-3-aminobenzamide

생성물 1

HCID 573315364-Ethynyl-3-nitrosobenzamide수율 12%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

0.46 g (2.87 mmol) 4-ethynyl-3-aminobenzamide (Compound XI-1), 10 ml water, were added into a 50 ml single-neck flask, then 1.2 g 58% sulfuric acid was added, and then 0.92 g 18.5% potassium dichromate solution. The mixture was stirred for 3 minutes until completing the reaction, extracted with ethyl acetate, dried over anhydrous sodium sulfate, and separated by column chromatography to obtain 0.06 g 4-ethynyl-3-nitrosobenzamide (Compound I-28, yellow-green solid), yield 12%, stored at −20° C.

후처리

  1. customthe reaction
  2. extractionextracted with ethyl acetate
  3. dry with materialdried over anhydrous sodium sulfate
  4. customseparated by column chromatography

출처 및 근거

ORD 기록
ord-c7902b96b07a4a119555f152276a1706
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08946478B2

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