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Water → methyl 1-benzyl-2-chloro-5-phenyl-1H-pyrrole-3-carboxylate

HRID 505821
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HRID 505821 반응식
[Cl:1][C:2]1[NH:3][C:4]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[CH:5][C:6]=1[C:7]([O:9][CH3:10])=[O:8].[H-].[Na+].[CH2:19](Br)[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1.O>CN(C=O)C>[CH2:19]([N:3]1[C:4]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[CH:5][C:6]([C:7]([O:9][CH3:10])=[O:8])=[C:2]1[Cl:1])[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1
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참가 물질

6

반응물 4

HCID 962WaterHCID 7498Benzyl BromideHCID 24758Sodium hydrideHCID 66974443methyl 2-chloro-5-phenyl-1H-pyrrole-3-carboxylate

생성물 1

HCID 68468834methyl 1-benzyl-2-chloro-5-phenyl-1H-pyrrole-3-carboxylate수율 71%

시약·촉매·용매 1

HCID 6228
Dimethylformamide
용매

실험 절차

A solution (7 M) of methyl 2-chloro-5-phenyl-1H-pyrrole-3-carboxylate in DMF at 0° C. was treated with NaH (1.2 eq., 60% dispersion in mineral oil), and the suspension was stirred at RT for 30 min then it was treated with benzyl bromide (1.2 eq.). The reaction mixture was stirred at RT for 90 min then poured into water and extracted with AcOEt. The combined organic phase was washed with water and dried. Evaporation of the solvent gave a residue that was purified by flash chromatography on silica gel (1:8 AcOEt/petroleum ether) to afford the title compound (71%) as a solid.

후처리

  1. stirringThe reaction mixture was stirred at RT for 90 min
  2. extractionextracted with AcOEt
  3. washThe combined organic phase was washed with water
  4. customdried
  5. customEvaporation of the solvent
  6. customgave a residue that
  7. customwas purified by flash chromatography on silica gel (1:8 AcOEt/petroleum ether)

출처 및 근거

ORD 기록
ord-0b88e83c557848fea88c13f6fb24b3ee
출처 데이터셋
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07781431B2

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