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HCID 178419731, 화합물 → 2-Bromo-3-nitro-5-(trifluoromethyl)pyridine

HRID 444915
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HRID 444915 반응식
[N+:1]([C:4]1[C:5](O)=[N:6][CH:7]=[C:8]([C:10]([F:13])([F:12])[F:11])[CH:9]=1)([O-:3])=[O:2].O(Br)[Br:16].[P+5]>C(#N)C>[Br:16][C:5]1[C:4]([N+:1]([O-:3])=[O:2])=[CH:9][C:8]([C:10]([F:13])([F:12])[F:11])=[CH:7][N:6]=1
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참가 물질

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HCID 178419731HCID 178419731, 화합물HCID 178526653HCID 178526653, 화합물

생성물 1

HCID 463152002-Bromo-3-nitro-5-(trifluoromethyl)pyridine

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

3-Nitro-5-(trifluoromethyl)pyridin-2-ol (31.00 g, 149 mmol) was dissolved in acetonitrile (250 ml) to give a dark brown solution. Phosphorus(V) oxybromide (85 g, 298 mmol) was added and the mixture was heated at reflux for 4.5 hours and then stirred at RT overnight. The reaction mixture was quenched by pouring into vigorously stirring water (600 ml) containing sodium hydrogencarbonate (110 g). The dark brown mixture was extracted with DCM (3×200 ml) and the organic phase was washed with water (200 ml) and brine (100 ml), dried (MgSO4) and concentrated in vacuo to afford the title product as a brown oil. 1H-NMR: [400 MHz, CDCl3, δH, 8.87 (1H, d, J=1.4 Hz, ArH), 8.39 (1H, d, J=1.9 Hz, ArH).

후처리

  1. customto give a dark brown solution
  2. temperaturethe mixture was heated
  3. temperatureat reflux for 4.5 hours
  4. customThe reaction mixture was quenched
  5. additionby pouring into vigorously stirring water (600 ml)
  6. additioncontaining sodium hydrogencarbonate (110 g)
  7. extractionThe dark brown mixture was extracted with DCM (3×200 ml)
  8. washthe organic phase was washed with water (200 ml) and brine (100 ml)
  9. dry with materialdried (MgSO4)
  10. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-c3fc454887404730b2acc39214a39a57
출처 데이터셋
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08476269B2

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