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Methanol → HCID 18787032, 화합물

HRID 1107281
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HRID 1107281 반응식
[Br:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[C:4]([CH2:11][CH:12]=C)[C:3]=1[OH:14].C[OH:16]>ClCCl>[Br:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[C:4]([CH2:11][CH2:12][OH:16])[C:3]=1[OH:14]
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참가 물질

4

반응물 2

HCID 887MethanolHCID 18787027HCID 18787027, 화합물

생성물 1

HCID 18787032HCID 18787032, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

2-Bromo-6-prop-2-enyl-4-nitrophenol (5.8 g) was dissolved in dichloromethane (30 ml) and methanol (30 ml) and the resulting solution was cooled to -78° C. Ozone was bubbled through the solution until a faint blue coloration was observed and all starting material had reacted. The solution was purged with nitrogen, sodium borohydride (850 g) was added and the solution was allowed to come to room temperature. The solvent was evaporated and the residue was dispersed between ethyl acetate and HCl (1N). The ethyl acetate layer was washed with water, brine, dried (MgSO4) and concentrated. The residue was purified on silica using 2% methanol in dichloromethane as eluent to afford the title compound as a white solid (4 g). 1H NMR (360 MHz, CDCl3) δ 3.03 (2H, t, J=5.4 Hz), 4.06 (2H, t, J=5.5 Hz), 8.01 (1H, d, J=2.6 Hz), 8.35 (1H, d, J=2.6 Hz).

후처리

  1. customOzone was bubbled through the solution until a faint blue coloration
  2. customall starting material had reacted
  3. customThe solution was purged with nitrogen, sodium borohydride (850 g)
  4. additionwas added
  5. customto come to room temperature
  6. customThe solvent was evaporated
  7. additionthe residue was dispersed between ethyl acetate and HCl (1N)
  8. washThe ethyl acetate layer was washed with water, brine
  9. dry with materialdried (MgSO4)
  10. concentrationconcentrated
  11. customThe residue was purified on silica using 2% methanol in dichloromethane as eluent

출처 및 근거

ORD 기록
ord-79f0a4a66ab1480eb902f81fde014a4a
출처 데이터셋
uspto-grants-2000_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06060469

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