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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Sodium Iodide → Noradenalone hydrochloride

HRID 346400
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HRID 346400 반응식
[Cl:1][CH2:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([OH:11])=[C:7]([OH:12])[CH:6]=1)=[O:4].[I-].[Na+].[N-:15]=[N+]=[N-].[Na+]>CC(C)=O>[ClH:1].[NH2:15][CH2:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([OH:11])=[C:7]([OH:12])[CH:6]=1)=[O:4]
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참가 물질

5

반응물 3

HCID 5238Sodium IodideHCID 33557Sodium AzideHCID 668342-Chloro-3',4'-dihydroxyacetophenone

생성물 1

HCID 199831Noradenalone hydrochloride수율 50.4%

시약·촉매·용매 1

HCID 180Acetone용매

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온도
40 °C

실험 절차

10 g (53.6 mmol) of 2-chloro-3',4'-dihydroxyacetophenone was dissolved in 50 ml of acetone, and 600 mg (4.0 mmol) of sodium iodide and 5.23 g (80.5 mmol) of sodium azide were added thereto. The mixture was refluxed for 24 hours. Insoluble substances in the reaction solution were filtered off and concentrated under reduced pressure. Ethyl acetate was added to the reaction solution, and washed sequentially with water and a saturated sodium chloride aqueous solution, and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. The oily residue was dissolved in 100 ml of methanol and 13.6 ml of concentrated hydrochloric acid, and 1.5 g of a 10% palladium carbon catalyst was added thereto. The mixture was stirred at 40° C. for 5 hours under hydrogen gas atmosphere. The reaction solution was filtered and the filtrate was concentrated under reduced pressure. To the concentrated residue, acetone was added, and the precipitated crystals were collected by filtration to obtain 5.5 g (yield: 50.4%) of 2-amino-3',4'-dihydroxyacetophenone hydrochloride.

후처리

  1. temperatureThe mixture was refluxed for 24 hours
  2. filtrationInsoluble substances in the reaction solution were filtered off
  3. concentrationconcentrated under reduced pressure
  4. additionEthyl acetate was added to the reaction solution
  5. washwashed sequentially with water
  6. dry with materiala saturated sodium chloride aqueous solution, and dried over anhydrous sodium sulfate
  7. distillationThe solvent was distilled off under reduced pressure
  8. dissolutionThe oily residue was dissolved in 100 ml of methanol
  9. addition13.6 ml of concentrated hydrochloric acid, and 1.5 g of a 10% palladium carbon catalyst was added
  10. filtrationThe reaction solution was filtered
  11. concentrationthe filtrate was concentrated under reduced pressure
  12. additionTo the concentrated residue, acetone was added
  13. filtrationthe precipitated crystals were collected by filtration

출처 및 근거

ORD 기록
ord-5fc28a9379414b758a2b0c538c963297
출처 데이터셋
uspto-grants-1991_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05061794

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