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Hydrochloric Acid → 3-Bromo-2,4-dichloro-5-fluoroaniline

HRID 1761645
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HRID 1761645 반응식
Cl.C(O)C.[Br:5][C:6]1[C:7]([Cl:17])=[C:8]([N+:14]([O-])=O)[CH:9]=[C:10]([F:13])[C:11]=1[Cl:12]>O.[Fe]>[Br:5][C:6]1[C:7]([Cl:17])=[C:8]([CH:9]=[C:10]([F:13])[C:11]=1[Cl:12])[NH2:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 702EthanolHCID 137487963-Bromo-2,4-dichloro-5-fluoronitrobenzene

생성물 1

HCID 137487973-Bromo-2,4-dichloro-5-fluoroaniline수율 72.2%

시약·촉매·용매 2

HCID 23925Iron촉매HCID 962Water용매

실험 절차

To a suspension of iron powder (135.4 g) in water (140 ml), with vigorous stirring at 50°-60° C., was slowly added concentrated hydrochloric acid (18 ml). After ethanol (350 ml) was mixed, 3-bromo-2,4-dichloro-5-fluoronitrobenzene (218.8 g) was added portionwise to the suspension at 52°-76° C. during an hour. After stirring for 75 minutes at the same temperature, the hot reaction mixture was filtered after adding benzene (500 ml) and the insoluble material was successively washed with hot ethanol (100 ml) and benzene (200 ml). The filtrate and washings were combined. The organic layers were washed with water saturated with sodium chloride, dried over anhydrous sodium sulfate and then concentrated. The resulting residue was recrystallized from ethanol-water to give the title compound (141.6 g) as light brown needles, mp 126°-129.5° C.

후처리

  1. stirringAfter stirring for 75 minutes at the same temperature
  2. filtrationthe hot reaction mixture was filtered
  3. additionafter adding benzene (500 ml)
  4. washthe insoluble material was successively washed with hot ethanol (100 ml) and benzene (200 ml)
  5. washThe organic layers were washed with water saturated with sodium chloride
  6. dry with materialdried over anhydrous sodium sulfate
  7. concentrationconcentrated
  8. customThe resulting residue was recrystallized from ethanol-water

출처 및 근거

ORD 기록
ord-4d07673edfc54c26b71ae4d7adff89bf
출처 데이터셋
uspto-grants-1989_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04826982

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