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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → 5-Methoxybenzo[d]isoxazol-3-amine

HRID 2396724
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HRID 2396724 반응식
[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([O:11][N:12]=C(C)C)=[C:7]([CH:10]=1)[C:8]#[N:9].Cl.C(=O)([O-])[O-].[Na+].[Na+]>CO>[NH2:9][C:8]1[C:7]2[CH:10]=[C:3]([O:2][CH3:1])[CH:4]=[CH:5][C:6]=2[O:11][N:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 10340Sodium CarbonateHCID 18796463HCID 18796463, 화합물

생성물 1

HCID 187964535-Methoxybenzo[d]isoxazol-3-amine수율 84.6%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

In 125 ml of dry methanol was dissolved 5-methoxy-2-[[(1-methylethylidene)amino]oxy]benzonitrile (10 g), followed by 125 ml of ethereal hydrochloric acid. The reaction was stirred under nitrogen overnight. The reaction was neutralized with saturated sodium carbonate solution and extracted with EtOAc. The organic layer was dried and concentrated in vacuo. Recrystallization of the residue from dichloromethane/petroleum ether afforded the expected product (6.8 g).

후처리

  1. extractionextracted with EtOAc
  2. customThe organic layer was dried
  3. concentrationconcentrated in vacuo
  4. customRecrystallization of the residue from dichloromethane/petroleum ether

출처 및 근거

ORD 기록
ord-b360e6a9610048b8b52c5103e03dbc53
출처 데이터셋
uspto-grants-1996_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05494908

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