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Hydrazine, dihydrochloride → HCID 15480333, 화합물

HRID 1741255
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HRID 1741255 반응식
[CH2:1]([CH:3]([C:11](=O)[C:12]1[C:17]([CH3:18])=[CH:16][C:15]([CH3:19])=[CH:14][C:13]=1[CH3:20])[C:4](=O)[C:5]([O:7][CH2:8][CH3:9])=[O:6])[CH3:2].Cl.Cl.[NH2:24][NH2:25]>CCO>[CH2:1]([C:3]1[C:11]([C:12]2[C:17]([CH3:18])=[CH:16][C:15]([CH3:19])=[CH:14][C:13]=2[CH3:20])=[N:24][NH:25][C:4]=1[C:5]([O:7][CH2:8][CH3:9])=[O:6])[CH3:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 17548Hydrazine, dihydrochlorideHCID 15870414HCID 15870414, 화합물

생성물 1

HCID 15480333HCID 15480333, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
80 °C

실험 절차

A mixture of ethyl 3-ethyl-2,4-dioxo-4-(2,4,6trimethylphenyl)butanoate (6.0 g, 20.7 mmol) and hydrazine dihydrochloride (2.17 g, 20.7 mmoL) in 100 mL of EtOH was stirred at 80° C. for 6 hours. The solvent was then removed from the mixture. 200 mL of water was added to the residue and mixture was neutralized by the addition of solid NaHCO3. The product was extracted into ether. The ether extract was dried over Na2SO4 and evaporated to give 5.8 g as an oil which was used in the next reaction without farther purification.

후처리

  1. customThe solvent was then removed from the mixture
  2. addition200 mL of water was added to the residue and mixture
  3. additionwas neutralized by the addition of solid NaHCO3
  4. extractionThe product was extracted into ether
  5. extractionThe ether extract
  6. dry with materialwas dried over Na2SO4
  7. customevaporated
  8. customto give 5.8 g as an oil which
  9. customwas used in the next reaction without farther purification

출처 및 근거

ORD 기록
ord-5616ef379a354c0facc65c10679039f9
출처 데이터셋
uspto-grants-1999_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05973152

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