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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → HCID 59367709, 화합물

HRID 1253594
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HRID 1253594 반응식
C([O-])(=O)C.[Na+].[F:6][C:7]1[CH:12]=[CH:11][C:10]([C:13](=[O:21])[CH2:14][C:15]2[CH:20]=[CH:19][N:18]=[N:17][CH:16]=2)=[CH:9][CH:8]=1.[Br:22]Br.O>C(O)(=O)C>[Br:22][CH:14]([C:15]1[CH:20]=[CH:19][N:18]=[N:17][CH:16]=1)[C:13]([C:10]1[CH:9]=[CH:8][C:7]([F:6])=[CH:12][CH:11]=1)=[O:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 24408BromineHCID 517045Sodium AcetateHCID 59367711HCID 59367711, 화합물

생성물 1

HCID 59367709HCID 59367709, 화합물

시약·촉매·용매 1

HCID 176Acetic Acid용매2회

실험 절차

0.70 g (5.2 mmol) of sodium acetate is added to a solution of 1.02 g (4.70 mmol) of 1-(4-fluorophenyl)-2-pyridazin-4-ylethanone in 20 ml of acetic acid and then 0.26 ml (5.2 mmol) of bromine in solution in a few ml of acetic acid is added dropwise (slight exotherm). After 30 minutes at ambient temperature, the reaction medium is cooled and 60 ml of water are added. The product is extracted with diethyl ether. The cooled organic phase is washed with an aqueous solution of sodium hydrogen carbonate, dried over sodium sulfate and filtered. This solution (approximately 50 ml) is used rapidly, as it is, in the rest of the synthesis.

후처리

  1. temperaturethe reaction medium is cooled
  2. extractionThe product is extracted with diethyl ether
  3. washThe cooled organic phase is washed with an aqueous solution of sodium hydrogen carbonate
  4. dry with materialdried over sodium sulfate
  5. filtrationfiltered
  6. customis, in the rest of the synthesis

출처 및 근거

ORD 기록
ord-e1780d54aee84703b61d29d8cb0eb967
출처 데이터셋
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08455491B2

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