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N-Hydroxyphthalimide → 2-[(5-Methyl-1H-imidazol-4-yl)methoxy]-1H-isoindole-1,3(2H)-dione

HRID 746318
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HRID 746318 반응식
[Na].[OH:2][N:3]1[C:7](=[O:8])[C:6]2=[CH:9][CH:10]=[CH:11][CH:12]=[C:5]2[C:4]1=[O:13].Cl.[CH3:15][C:16]1[NH:20][CH:19]=[N:18][C:17]=1[CH2:21]Cl>C(O)C>[CH3:15][C:16]1[NH:20][CH:19]=[N:18][C:17]=1[CH2:21][O:2][N:3]1[C:4](=[O:13])[C:5]2=[CH:12][CH:11]=[CH:10][CH:9]=[C:6]2[C:7]1=[O:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 10665N-HydroxyphthalimideHCID 5360545SodiumHCID 124562084-(Chloromethyl)-5-methyl-1H-imidazole--hydrogen chloride (1/1)

생성물 1

HCID 137520522-[(5-Methyl-1H-imidazol-4-yl)methoxy]-1H-isoindole-1,3(2H)-dione수율 48.7%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of 1 g of sodium and 80 ml of ethanol was cooled in an ice-bath and 7.12 g of N-hydroxyphthalimide was added thereto and the mixture was stirred at room temperature. The mixture was cooled in an ice-bath and 3.16 g of 5-methyl-4-chloromethylimidazole hydrochloride was added thereto. The resulting mixture was stirred for 2 hours. The solvent was distilled off and SSB was added to the residue and the mixture was extracted with chloroform. The extract was washed with SSC and dried with sodium sulfate and concentrated to dryness. The residue was washed with ether to give 2.37 g of N-((5-methylimidazole-4-yl)methoxy)phthalimide with mp 155°-156° C.

후처리

  1. temperaturewas cooled in an ice-bath
  2. temperatureThe mixture was cooled in an ice-bath
  3. stirringThe resulting mixture was stirred for 2 hours
  4. distillationThe solvent was distilled off
  5. additionSSB was added to the residue
  6. extractionthe mixture was extracted with chloroform
  7. washThe extract was washed with SSC
  8. dry with materialdried with sodium sulfate
  9. concentrationconcentrated to dryness
  10. washThe residue was washed with ether

출처 및 근거

ORD 기록
ord-fc53f7533bca40e98258263b3691896b
출처 데이터셋
uspto-grants-1986_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04603198

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