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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Diisopropyl Ether → R 57720

HRID 1719254
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HRID 1719254 반응식
[N+]([O-])(O)=O.[Cl:5]/[C:6](/[C:13]1[CH:18]=[CH:17][C:16]([Cl:19])=[CH:15][C:14]=1[Cl:20])=[CH:7]\[N:8]1[CH:12]=[CH:11][N:10]=[CH:9]1.O(C(C)C)C(C)C.[OH-].[NH4+]>O>[ClH:5].[Cl:5]/[C:6](/[C:13]1[CH:18]=[CH:17][C:16]([Cl:19])=[CH:15][C:14]=1[Cl:20])=[CH:7]\[N:8]1[CH:12]=[CH:11][N:10]=[CH:9]1
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참가 물질

5

반응물 3

HCID 7914Diisopropyl EtherHCID 14923Ammonium HydroxideHCID 86740282HCID 86740282, 화합물

생성물 1

HCID 3035789R 57720

시약·촉매·용매 1

HCID 962Water용매

실험 절차

To a stirred mixture of 12.76 parts of (Z)-1-[2-chloro-2-(2,4-dichlorophenyl)ethenyl]-1H-imidazole mononitrate, 120 parts of water and 70 parts of 2,2'-oxybispropane were added 3.5 parts of ammonium hydroxide. The whole was stirred till homogeneous. The layers were separated. The aqueous phase was extracted with 35 parts of 2,2'-oxybispropane. The combined organic layers were washed with water, dried, filtered and evaporated in vacuo. The residue was converted into the hydrochloride salt in 64 parts of 2-propanone. The salt was filtered off, washed with 2-propanone and dried in vacuo, yielding 8.54 parts of (Z)-1-[2-chloro-2-(2,4-dichlorophenyl)ethenyl]-1H-imidazole monohydrochloride; mp. 178.8° C. (compound 3).

후처리

  1. customThe layers were separated
  2. extractionThe aqueous phase was extracted with 35 parts of 2,2'-oxybispropane
  3. washThe combined organic layers were washed with water
  4. customdried
  5. filtrationfiltered
  6. customevaporated in vacuo
  7. filtrationThe salt was filtered off
  8. washwashed with 2-propanone
  9. customdried in vacuo

출처 및 근거

ORD 기록
ord-2bba09e56b5e4dab814eb3248e8032ed
출처 데이터셋
uspto-grants-1985_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04539325

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