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Ammonium Chloride → 2-(4-Methylphenyl)-1,3-benzoxazol-6-amine

HRID 1886913
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HRID 1886913 반응식
[N+:1]([C:4]1[CH:19]=[CH:18][C:7]2[N:8]=[C:9]([C:11]3[CH:16]=[CH:15][C:14]([CH3:17])=[CH:13][CH:12]=3)[O:10][C:6]=2[CH:5]=1)([O-])=O.[Cl-].[NH4+]>C(O)C.O.[Fe]>[C:14]1([CH3:17])[CH:13]=[CH:12][C:11]([C:9]2[O:10][C:6]3[CH:5]=[C:4]([NH2:1])[CH:19]=[CH:18][C:7]=3[N:8]=2)=[CH:16][CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 25517Ammonium ChlorideHCID 12251550HCID 12251550, 화합물

생성물 1

HCID 164792462-(4-Methylphenyl)-1,3-benzoxazol-6-amine수율 4%

시약·촉매·용매 2

HCID 23925Iron촉매HCID 19096565Water ethanol용매

실험 절차

To 6-nitro-2-p-tolylbenzo[d]oxazole (2.1 g, 8.27 mmol) in ethanol:water 2:1 v/v (60 mL) at 70° C. was added iron powder (2.14 g, 38.3 mmol) and ammonium chloride (819 mg, 15.3 mmol). The suspension was stirred at reflux for 16 h. After cooling, the solution was filtered through a pad of Celite® and washed with ethanol. After evaporation of the solvent, the aqueous layer was extracted twice with ethyl acetate. The combined organic layers were dried over anhydrous MgSO4 and evaporated. The resulting solid was purified by column chromatography eluting with ethyl acetate:hexanes 1:3 v/v to afford 70 mg (4%) of the title compound (LCMS RT=6.12 min, MH+ 223.1)

후처리

  1. temperatureat reflux for 16 h
  2. temperatureAfter cooling
  3. filtrationthe solution was filtered through a pad of Celite®
  4. washwashed with ethanol
  5. customAfter evaporation of the solvent
  6. extractionthe aqueous layer was extracted twice with ethyl acetate
  7. dry with materialThe combined organic layers were dried over anhydrous MgSO4
  8. customevaporated
  9. customThe resulting solid was purified by column chromatography
  10. washeluting with ethyl acetate:hexanes 1:3 v/v

출처 및 근거

ORD 기록
ord-2455ae1c656d43228a964f8aad46fc9d
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08501713B2

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