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Acetic Acid → 2-Methylbenzo[d]thiazol-7-amine

HRID 620120
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HRID 620120 반응식
[CH3:1][C:2]1[S:3][C:4]2[C:10]([N+:11]([O-])=O)=[CH:9][CH:8]=[CH:7][C:5]=2[N:6]=1.C(O)(=O)C>C(O)C.[Fe]>[CH3:1][C:2]1[S:3][C:4]2[C:10]([NH2:11])=[CH:9][CH:8]=[CH:7][C:5]=2[N:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 176Acetic AcidHCID 2764082-Methyl-7-nitro-1,3-benzothiazole

생성물 1

HCID 138244302-Methylbenzo[d]thiazol-7-amine수율 68.5%

시약·촉매·용매 2

HCID 23925Iron촉매HCID 702Ethanol용매

실험 절차

To a solution of 3.8 g of the product from Example 6 and 8.1 g of glacial acetic acid in 56 mL absolute ethanol at reflux temperature was added 3.8 g of iron powder in small portions. The reaction mixture was heated at reflux temperature for about 36 hours, and was then cooled and filtered. The filtrate was concentrated in vacuo and the residue treated with several mL cold water to give a solid. Filtration and drying gave 2.2 g of the title compound as a tan-colored solid, m.p. 100°-101° C.; NMR (CDCl3): δ 2.8 (3H, s), 3.9 (2H, br s), 6.65 (1H, d, J=8 Hz), 7.2 (1H, t, J=8 Hz), 7.5 (1H, d, J=8 Hz).

후처리

  1. temperatureThe reaction mixture was heated
  2. temperatureat reflux temperature for about 36 hours
  3. temperaturewas then cooled
  4. filtrationfiltered
  5. concentrationThe filtrate was concentrated in vacuo
  6. additionthe residue treated with several mL cold water
  7. customto give a solid
  8. filtrationFiltration
  9. customdrying

출처 및 근거

ORD 기록
ord-3a33860c24b84efb96d85e611b174927
출처 데이터셋
uspto-grants-1989_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04820332

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