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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Ethanol → 2-chloro-6-fluoro-N'-hydroxybenzenecarboximidamide

HRID 2228858
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HRID 2228858 반응식
[Cl:1][C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([F:10])[C:3]=1[C:4]#[N:5].Cl.[NH2:12][OH:13].C(=O)([O-])[O-].[Na+].[Na+].C(O)C>O>[Cl:1][C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([F:10])[C:3]=1[C:4](=[N:12][OH:13])[NH2:5]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 702EthanolHCID 10340Sodium CarbonateHCID 695872-Chloro-6-fluorobenzonitrileHCID 443297Hydroxyamine hydrochloride

생성물 1

HCID 46234272-chloro-6-fluoro-N'-hydroxybenzenecarboximidamide

시약·촉매·용매 1

HCID 962Water용매

반응 조건

온도
72.5 °C

실험 절차

A mixture of 15.6 g of 2-chloro-6-fluorobenzonitrile, 9.0 g of hydroxylamine hydrochloride, 7.4 g of sodium carbonate, 50 ml of ethanol and 15 ml of water was stirred at 70-75° C. for 16 h. The solvent was evaporated and the residue was stirred with tertbutyl methyl ether, and the filtrate afforded, after evaporation of the solvent, 17.6 g of the desired product of m.p. 115-120° C.

후처리

  1. customThe solvent was evaporated
  2. stirringthe residue was stirred with tertbutyl methyl ether
  3. customthe filtrate afforded
  4. customafter evaporation of the solvent, 17.6 g of the desired product of m.p. 115-120° C.

출처 및 근거

ORD 기록
ord-5be28282c74240769217d730973e239e
출처 데이터셋
uspto-grants-2002_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06417398B1

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