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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Potassium Nitrate → 2H-3,1-Benzoxazin-2-one, 6-bromo-1,4-dihydro-5-methyl-8-nitro-

HRID 635807
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인쇄 미리보기

반응식

HRID 635807 반응식
[Br:1][C:2]1[CH:12]=[CH:11][C:5]2[NH:6][C:7](=[O:10])[O:8][CH2:9][C:4]=2[C:3]=1[CH3:13].[N+:14]([O-])([O-:16])=[O:15].[K+]>OS(O)(=O)=O>[Br:1][C:2]1[CH:12]=[C:11]([N+:14]([O-:16])=[O:15])[C:5]2[NH:6][C:7](=[O:10])[O:8][CH2:9][C:4]=2[C:3]=1[CH3:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24434Potassium NitrateHCID 107765166-Bromo-5-methyl-1H-benzo[d][1,3]oxazin-2(4H)-one

생성물 1

HCID 107556822H-3,1-Benzoxazin-2-one, 6-bromo-1,4-dihydro-5-methyl-8-nitro-

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

실험 절차

To a solution of 6-bromo-5-methyl-1,4-dihydro-benzo[d][1,3]oxazin-2-one (0.726 g, 3 mmol) in concentrate H2SO4 (4 mL), KNO3 (0.303 g, 3 mmol) was added at 0° C. Reaction mixture stirred 14 hours and poured over crushed ice. Yellow precipitate was obtained, which was filtered and dried.

후처리

  1. customReaction mixture
  2. additionpoured
  3. customover crushed ice
  4. customYellow precipitate was obtained
  5. filtrationwhich was filtered
  6. customdried

출처 및 근거

ORD 기록
ord-c532a7cb3a34411096b39986f6c8bbbe
출처 데이터셋
uspto-grants-2001_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06191134B1

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