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4-Chlorobenzaldehyde → HCID 178458262, 화합물

HRID 1418056
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인쇄 미리보기

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HRID 1418056 반응식
[CH2:1]([O:4][C:5]1[CH:10]=[C:9]([O:11][CH2:12][CH2:13][CH3:14])[CH:8]=[CH:7][C:6]=1[C:15](=O)[C:16]([C:18]1[CH:23]=[CH:22][N:21]=[CH:20][CH:19]=1)=O)[CH2:2][CH3:3].C([O-])(=O)C.[NH4+:29].[Cl:30][C:31]1[CH:38]=[CH:37][C:34]([CH:35]=O)=[CH:33][CH:32]=1.[OH-].[NH4+:40]>C(O)(=O)C.C(OCC)(=O)C>[Cl:30][C:31]1[CH:38]=[CH:37][C:34]([C:35]2[NH:29][C:16]([C:18]3[CH:23]=[CH:22][N:21]=[CH:20][CH:19]=3)=[C:15]([C:6]3[CH:7]=[CH:8][C:9]([O:11][CH2:12][CH2:13][CH3:14])=[CH:10][C:5]=3[O:4][CH2:1][CH2:2][CH3:3])[N:40]=2)=[CH:33][CH:32]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 77264-ChlorobenzaldehydeHCID 14923Ammonium HydroxideHCID 517165Ammonium AcetateHCID 53632863HCID 53632863, 화합물

생성물 1

HCID 178458262HCID 178458262, 화합물수율 30%

시약·촉매·용매 2

HCID 176Acetic Acid용매
HCID 8857
Ethyl Acetate
용매

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온도
0 °C

실험 절차

A solution of 1-(2,4-di-n-propyloxyphenyl)-2-(4-pyridyl)ethane-1,2-dione from Step D (61 mg, 0.19 mmol), ammonium acetate (144 mg, 1.87 mmol) and 4-chlorobenzaldehyde (33 mg, 0.23 mmol) in acetic acid (1.5 mL) was heated to 100° C. for 3.5 h. After cooling to 0° C., the ice (4g), ethyl acetate (2 mL) and a concentrated solution of ammonium hydroxide was added until the pH was 10. The layers were separated and the aqueous layer extracted with ethyl acetate. The combined organic extracts were successively washed with water and saturated salt solution and dried over anhydrous sodium sulfate. The mixture was filtered and the solvent removed by rotoevaporation. The residue was purified by flash column chromatography on silica gel eluted with 0-3% methanol in methylene chloride to yield the title compound as a cream-colored solid (25 mg, 30% yield), mass spectrum (CI) m/e=448 (M+1)+.

후처리

  1. customThe layers were separated
  2. extractionthe aqueous layer extracted with ethyl acetate
  3. washThe combined organic extracts were successively washed with water and saturated salt solution
  4. dry with materialdried over anhydrous sodium sulfate
  5. filtrationThe mixture was filtered
  6. customthe solvent removed by rotoevaporation
  7. customThe residue was purified by flash column chromatography on silica gel
  8. washeluted with 0-3% methanol in methylene chloride

출처 및 근거

ORD 기록
ord-dea4770b36114084b3806b9f609720f1
출처 데이터셋
uspto-grants-1999_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05880139

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