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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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tert-Butanol → HCID 12016671, 화합물

HRID 1830797
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인쇄 미리보기

반응식

HRID 1830797 반응식
CC(O)(C)C.[K].[Br:7][C:8]1[CH:13]=[CH:12][C:11]([NH:14][C:15](=[O:17])[CH3:16])=[C:10]([C:18](=O)[C:19]2[CH:24]=[CH:23][CH:22]=[C:21]([Cl:25])[CH:20]=2)[CH:9]=1>COCCOC>[Br:7][C:8]1[CH:9]=[C:10]2[C:11](=[CH:12][CH:13]=1)[NH:14][C:15](=[O:17])[CH:16]=[C:18]2[C:19]1[CH:24]=[CH:23][CH:22]=[C:21]([Cl:25])[CH:20]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6386tert-ButanolHCID 5462222PotassiumHCID 23248656HCID 23248656, 화합물

생성물 1

HCID 12016671HCID 12016671, 화합물수율 80.76%

시약·촉매·용매 1

HCID 80711,2-Dimethoxyethane용매

실험 절차

2-methyl,2-propanol, potassium salt (1.635 mol) was added portionwise at room temperature to a solution of intermediate (3) (0.328 mol) in DME (1200 ml) and the mixture was stirred at room temperature for one night. The mixture was evaporated till dryness, the residue was poured into water and ice and decanted. The oily residue was taken up in DIPE, the precipitate was filtered off, washed with EtOAc, CH3CN and diethylether and dried, yielding 88.6 g (80.76%) of 6-bromo-4-(3-chlorophenyl)-2(1H)-quinolinone (intermediate 4).

후처리

  1. customThe mixture was evaporated till dryness
  2. additionthe residue was poured into water and ice
  3. customdecanted
  4. filtrationthe precipitate was filtered off
  5. washwashed with EtOAc, CH3CN and diethylether
  6. customdried

출처 및 근거

ORD 기록
ord-9078ec70312540b1a21e0ea04a11775c
출처 데이터셋
uspto-grants-2006_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07067531B2

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