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Hydrochloric Acid → 2,7-Diamino-9-fluorenone

HRID 1241223
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HRID 1241223 반응식
[N+:1]([C:4]1[CH:16]=[CH:15][C:14]2[C:13]3[C:8](=[CH:9][C:10]([N+:17]([O-])=O)=[CH:11][CH:12]=3)[C:7](=[O:20])[C:6]=2[CH:5]=1)([O-])=O.Cl>C(O)(=O)C>[NH2:1][C:4]1[CH:16]=[CH:15][C:14]2[C:13]3[C:8](=[CH:9][C:10]([NH2:17])=[CH:11][CH:12]=3)[C:7](=[O:20])[C:6]=2[CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 358422,7-Dinitro-9-fluorenone

생성물 1

HCID 972382,7-Diamino-9-fluorenone

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

2,7-Dinitro-9-fluorenone (162 g, 0.6 mol, from Aldrich) was added cautiously to a solution of hydrated stannous chloride (1100 g, 4.9 mol, from Aldrich) in a mixture of concentrated hydrochloric acid (900 ml) and acetic acid (1600 ml). The suspension was stirred and refluxed for 1 hour. The mixture was cooled to room temperature, and a solid appeared. The solid was harvested by filtration. The solid was washed first with concentrated hydrochloric acid, and then with water until the filtrate color was violet. The residue was dissolved in boiling water. The solution was filtered and then made alkaline with sodium hydroxide to from a precipitate. The precipitate was washed with water, dried, and recrystallized from dioxane. The yield of 2,7-diamino-9-fluorenone was 108 g (85.7%). The melting point was found to be 284–286° C.

후처리

  1. temperaturerefluxed for 1 hour
  2. filtrationThe solid was harvested by filtration
  3. washThe solid was washed first with concentrated hydrochloric acid
  4. dissolutionThe residue was dissolved
  5. filtrationThe solution was filtered
  6. washThe precipitate was washed with water
  7. customdried
  8. customrecrystallized from dioxane
  9. customto be 284–286° C.

출처 및 근거

ORD 기록
ord-e15ba46c9c9d4874b664005182bcc2de
출처 데이터셋
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07115347B2

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