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1,3-Dibromopropane → 8-(3-bromopropoxycarbonyl)-3-methyl-4-oxo-2-phenyl-4H-1-benzopyran

HRID 2400161
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HRID 2400161 반응식
[Br:1][CH2:2][CH2:3][CH2:4]Br.[CH3:6][C:7]1[C:12](=[O:13])[C:11]2[CH:14]=[CH:15][CH:16]=[C:17]([C:18]([O-:20])=[O:19])[C:10]=2[O:9][C:8]=1[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1.[Na+]>CN(C)C=O.O>[Br:1][CH2:2][CH2:3][CH2:4][O:20][C:18]([C:17]1[C:10]2[O:9][C:8]([C:21]3[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=3)=[C:7]([CH3:6])[C:12](=[O:13])[C:11]=2[CH:14]=[CH:15][CH:16]=1)=[O:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 80011,3-DibromopropaneHCID 236933394h-1-benzopyran-8-carboxylic acid, 3-methyl-4-oxo-2-phenyl-, sodium salt

생성물 1

HCID 199726458-(3-bromopropoxycarbonyl)-3-methyl-4-oxo-2-phenyl-4H-1-benzopyran수율 69.6%

시약·촉매·용매 2

HCID 962Water용매2회HCID 6228Dimethylformamide용매

실험 절차

30 g of 1,3-dibromopropane was added dropwise at ambient temperature to a suspension of 30 g of sodium 3-methyl-4-oxo-2-phenyl-4H-1-benzopyran-8-carboxylate in 150 ml of dimethylformamide and 35 ml of water. The reaction mixture was stirred at ambient temperature for 5 days. 100 ml of water were added and stirring was continued for another 15 minutes. The precipitate was filtered by suction, washed with water and purified by flash chromatography on silica gel, eluting with chloroform:ethyl acetate 95:5. The collected fractions were evaporated to dryness in vacuo and the residue was recrystallized from ethanol to give 27.7 g of the title compound, melting point 114°-115° C.

후처리

  1. stirringstirring
  2. waitwas continued for another 15 minutes
  3. filtrationThe precipitate was filtered by suction
  4. washwashed with water
  5. custompurified by flash chromatography on silica gel
  6. washeluting with chloroform:ethyl acetate 95:5
  7. customThe collected fractions were evaporated to dryness in vacuo
  8. customthe residue was recrystallized from ethanol

출처 및 근거

ORD 기록
ord-8e57a27e8c154aa0a2dc832a7b0cc9d4
출처 데이터셋
uspto-grants-1995_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05453518

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