Trifluoroacetic acid → Methyl 8-bromo-1,2,3,4-tetrahydro-1-benzazocine-5-carboxylate

HRID 1928940노트

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HRID 1928940 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[N:12](CC3C=CC(OC)=CC=3)[CH2:11][CH2:10][CH2:9][C:8]([C:22]([O:24][CH3:25])=[O:23])=[CH:7][C:6]=2[CH:26]=1.FC(F)(F)C(O)=O>C1(C)C=CC=CC=1>[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[NH:12][CH2:11][CH2:10][CH2:9][C:8]([C:22]([O:24][CH3:25])=[O:23])=[CH:7][C:6]=2[CH:26]=1

참가 물질

4

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온도
65 °C

실험 절차

To a solution of methyl 8-bromo-1-(4-methoxybenzyl)-1,2,3,4-terahydro-1-benzoazocine-5-carboxylate (10.0 g), in toluene (50 ml) was added trifluoroacetic acid (50 ml), and the mixture was stirred at 65° C. for 2 hours. After distilling off the solvent under reduced pressure, water was added at 0° C. and the reaction mixture was neutralized with potassium carbonate and extracted with ethyl acetate. The organic layer was washed with aqueous saturated sodium bicarbonate solution and saturated brine, after which it was dried with magnesium sulfate. The solvent was distilled off under reduced pressure, and the resulting residue was purified by basic silica gel column chromatography (hexane:ethyl acetate=9:1). The resulting solid was washed with hexane to give methyl 8-bromo-1,2,3,4-terahydro-1-benzoazocine-5-carboxylate (6.59 g) as yellow crystals.

후처리

  1. distillationAfter distilling off the solvent under reduced pressure, water
  2. additionwas added at 0° C.
  3. extractionextracted with ethyl acetate
  4. washThe organic layer was washed with aqueous saturated sodium bicarbonate solution and saturated brine
  5. dry with materialafter which it was dried with magnesium sulfate
  6. distillationThe solvent was distilled off under reduced pressure
  7. customthe resulting residue was purified by basic silica gel column chromatography (hexane:ethyl acetate=9:1)
  8. washThe resulting solid was washed with hexane

출처 및 근거

ORD 기록
ord-7ad61db351194b358a630d41ef563d8d
출처 데이터셋
uspto-grants-2012_05
특허 번호
US08183273B2

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