홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Acetone → ethyl 2-(1-isopropoxycarbonyloxy-2-methylpropyl)-5-(5-isopropoxy-4-methoxy-2-nitrobenzoyl)-2H-1,2,3-triazole-4-carboxylate

HRID 1794701
노트
인쇄 미리보기

반응식

HRID 1794701 반응식
[I-].[Na+].[C:3](=[O:6])([O-])[O-].[K+].[K+].Cl[C:10]([O:12][CH:13]([CH3:15])[CH3:14])=[O:11].[CH:16]([O:19][C:20]1[C:21]([O:41][CH3:42])=[CH:22][C:23]([N+:38]([O-:40])=[O:39])=[C:24]([CH:37]=1)[C:25]([C:27]1[NH:31][N:30]=[N:29][C:28]=1[C:32]([O:34][CH2:35][CH3:36])=[O:33])=[O:26])([CH3:18])[CH3:17].[CH3:43][C:44]([CH3:46])=O>O>[CH:13]([O:12][C:10]([O:6][CH:3]([N:30]1[N:29]=[C:28]([C:32]([O:34][CH2:35][CH3:36])=[O:33])[C:27]([C:25](=[O:26])[C:24]2[CH:37]=[C:20]([O:19][CH:16]([CH3:18])[CH3:17])[C:21]([O:41][CH3:42])=[CH:22][C:23]=2[N+:38]([O-:40])=[O:39])=[N:31]1)[CH:44]([CH3:46])[CH3:43])=[O:11])([CH3:15])[CH3:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 180AcetoneHCID 5238Sodium IodideHCID 7917Isopropyl chloroformateHCID 11430Potassium CarbonateHCID 178470513HCID 178470513, 화합물

생성물 1

HCID 22222605ethyl 2-(1-isopropoxycarbonyloxy-2-methylpropyl)-5-(5-isopropoxy-4-methoxy-2-nitrobenzoyl)-2H-1,2,3-triazole-4-carboxylate
수율 89%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

Isobutyl aldehyde (2.9 ml), sodium iodide (3.18 g), potassium carbonate (11.69 g), and isopropyl chloroformate (7.2 ml) were added in that order under an argon atmosphere at room temperature to a solution of ethyl 5-(5-isopropoxy-4-methoxy-2-nitrobenzoyl)-1H-1,2,3-triazole-4-carboxylate (8.01 g), prepared in step (32a), in acetone (150 ml). The mixture was stirred at that temperature for 19.5 hr. Water was added to the reaction mixture to stop the reaction. The mixture was extracted with ethyl acetate. The organic layer was washed with 20% saline and dried over anhydrous magnesium sulfate. The solvent was evaporated. The resultant mixture was purified by column chromatography on silica gel (hexane/ethyl acetate) to give ethyl 2-(1-isopropoxycarbonyloxy-2-methylpropyl)-5-(5-isopropoxy-4-methoxy-2-nitrobenzoyl)-2H-1,2,3-triazole-4-carboxylate (10.12 g, 89%).

후처리

  1. customthe reaction
  2. extractionThe mixture was extracted with ethyl acetate
  3. washThe organic layer was washed with 20% saline
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customThe solvent was evaporated
  6. customThe resultant mixture was purified by column chromatography on silica gel (hexane/ethyl acetate)

출처 및 근거

ORD 기록
ord-3267b2e8cb374f3fa9aa7e9afa845619
출처 데이터셋
uspto-grants-2006_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07022860B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트