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Ethanol → HCID 71744029, 화합물

HRID 402959
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HRID 402959 반응식
[Br:1][C:2]1[CH:3]=[C:4]([N+:12]([O-])=O)[CH:5]=[C:6]2[C:11]=1[N:10]=[CH:9][CH:8]=[CH:7]2.[Cl-].[NH4+].C(O)C>[Fe].O>[Br:1][C:2]1[CH:3]=[C:4]([NH2:12])[CH:5]=[C:6]2[C:11]=1[N:10]=[CH:9][CH:8]=[CH:7]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 702EthanolHCID 25517Ammonium ChlorideHCID 141173628-Bromo-6-nitroquinoline

생성물 1

HCID 71744029HCID 71744029, 화합물수율 47.6%

시약·촉매·용매 2

HCID 23925Iron촉매HCID 962Water용매

실험 절차

To a flask containing 8-bromo-6-nitroquinoline (2.05 g, 8.1 mmol), electrolytic iron (2.26 g, 40.5 mmol) and ammonium chloride (2.25 g, 42.1 mmol) was added ethanol (20 ml) and water (10 ml). The flask was fitted with an efficient reflux condenser and then heated to near reflux (oil bath) for 3 hours. The hot material was then filtered through a plug of celite and rinsed well with hot methanol (100 ml). The solvent was removed. The residue was taken up in ethyl acetate (60 ml) and water (60 ml) and transferred to a separatory funnel, agitated and the organic phase collected. The organic phase was washed with an equal volume of brine. The aqueous phases were back extracted with ethyl acetate (2×50 ml). The combined ethyl acetate extracts were dried over MgSO4, and concentrated in vacuo. The resulting residue was crystallized from hot dichloromethane/hexanes to provide the desired product as a brown powder (860 mg).

후처리

  1. customThe flask was fitted with an efficient reflux condenser
  2. temperatureheated
  3. temperatureto near reflux (oil bath) for 3 hours
  4. filtrationThe hot material was then filtered through a plug of celite
  5. washrinsed well with hot methanol (100 ml)
  6. customThe solvent was removed
  7. customwater (60 ml) and transferred to a separatory funnel
  8. customthe organic phase collected
  9. washThe organic phase was washed with an equal volume of brine
  10. extractionThe aqueous phases were back extracted with ethyl acetate (2×50 ml)
  11. dry with materialThe combined ethyl acetate extracts were dried over MgSO4
  12. concentrationconcentrated in vacuo
  13. customThe resulting residue was crystallized from hot dichloromethane/hexanes

출처 및 근거

ORD 기록
ord-834544517acd4a14b028d9f174698639
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08742098B2

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