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Ethanol → HCID 14274201, 화합물

HRID 1032003
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인쇄 미리보기

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HRID 1032003 반응식
[CH3:1][S:2]([NH:5][C:6]1[CH:15]=[CH:14][CH:13]=[C:12]2[C:7]=1[CH:8]=[CH:9][CH:10]=[C:11]2[OH:16])(=[O:4])=[O:3].C(O)C.[N:20]([O-])=[O:21].[Na+]>O.[Cl-].[Zn+2].[Cl-]>[N:20]([C:10]1[CH:9]=[CH:8][C:7]2[C:12](=[CH:13][CH:14]=[CH:15][C:6]=2[NH:5][S:2]([CH3:1])(=[O:4])=[O:3])[C:11]=1[OH:16])=[O:21]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 702EthanolHCID 104704Methanesulfonamide, N-(5-hydroxy-1-naphthalenyl)-HCID 23668193Sodium Nitrite

생성물 1

HCID 14274201HCID 14274201, 화합물

시약·촉매·용매 2

HCID 3007855Zincchloride촉매HCID 962Water용매2회

반응 조건

온도
50 °C

실험 절차

A mixture comprising 119 g of 5-methanesulfonylamino-1-naphthol, 100 g of zinc chloride and 500 ml of ethanol was heated at 50° C., and then a solution of 35 g of sodium nitrite as dissolved in 70 ml of water was added dropwise thereto at 50° to 65° C. After being heated and stirred at 60° to 65° C. for 2 hours, the resulting solution was cooled with water to room temperature, and reddish brown crystals formed were taken out by filtration and washed with ethanol. The crystals were added to 200 ml of concentrated hydrochloric acid and stirred for 1 hour at room temperature, and then 200 ml of water was added thereto. Yellowish brown crystals (2-nitroso-5-methanesulfonylamino-1-naphthol) formed were taken out by filtration, washed with water and dried. Yield: 90 g.

후처리

  1. additionwas added dropwise
  2. customat 50° to 65° C
  3. temperatureAfter being heated
  4. customformed
  5. filtrationwere taken out by filtration
  6. washwashed with ethanol
  7. additionThe crystals were added to 200 ml of concentrated hydrochloric acid
  8. stirringstirred for 1 hour at room temperature
  9. addition200 ml of water was added

출처 및 근거

ORD 기록
ord-9abec76542314cb5849ae40ff6f0558d
출처 데이터셋
uspto-grants-1990_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04956456

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