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Tri-o-tolylphosphine → HCID 22132398, 화합물

HRID 1856685
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HRID 1856685 반응식
C1(C)C=CC=CC=1P(C1C=CC=CC=1C)C1C=CC=CC=1C.[CH2:23]1[CH2:32][O:31][C:30]2[CH:29]=[CH:28][C:27](Br)=[CH:26][C:25]=2[O:24]1.[N:34]1[CH:39]=[CH:38][CH:37]=[C:36]([CH2:40][CH2:41][CH:42]([OH:45])[CH:43]=[CH2:44])[CH:35]=1>C(N(CC)CC)C.C(#N)C.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[O:31]1[C:30]2[CH:29]=[CH:28][C:27]([CH2:44][CH2:43][C:42](=[O:45])[CH2:41][CH2:40][C:36]3[CH:35]=[N:34][CH:39]=[CH:38][CH:37]=3)=[CH:26][C:25]=2[O:24][CH2:23][CH2:32]1.[O:31]1[C:30]2[CH:29]=[CH:28][C:27](/[CH:44]=[CH:43]/[CH:42]([OH:45])[CH2:41][CH2:40][C:36]3[CH:35]=[N:34][CH:39]=[CH:38][CH:37]=3)=[CH:26][C:25]=2[O:24][CH2:23][CH2:32]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 3

HCID 80271Tri-o-tolylphosphineHCID 1041416-Bromo-1,4-benzodioxaneHCID 17866850HCID 17866850, 화합물

생성물 2

HCID 22132398HCID 22132398, 화합물HCID 22132429HCID 22132429, 화합물

시약·촉매·용매 3

HCID 167845palladium(II) acetate촉매
HCID 6342
Acetonitrile
용매
HCID 8471Triethylamine용매

반응 조건

온도
80 °C

실험 절차

A mixture of palladium(II) acetate (0.112 g), tri-o-tolylphosphine (0.304 g), 3,4-ethylenedioxybromobenzene (1.075 g) and (±)-5-(pyridin-3-yl)-1-penten-3-ol (0.815 g, Example 1a)) in triethylamine (10 ml) in acetonitrile (30 ml) was heated at 80° C. for 3 hours and 30 minutes. The mixture was cooled to room temperature and filtered through Celite® and the filtrate concentrated under reduced pressure. The residue was redissolved in ethyl acetate and the solution washed with water then dried over anhydrous magnesium sulfate. The solution was then filtered and concentrated under reduced pressure. The residue was purified by column chromatography over silica eluting with hexane:acetone (3:1) then (2:1) to give firstly 1-(benzo-1,4-dioxan-6-yl)-5-(pyridin-3-yl)-3-pentanone as an oil (0.812 g) and secondly (±)-trans-1-(benzo-1,4-dioxan-6-yl)-5-(pyridin-3-yl)-pent-1-en-3-ol as an oil (0.252 g).

후처리

  1. temperatureThe mixture was cooled to room temperature
  2. filtrationfiltered through Celite®
  3. concentrationthe filtrate concentrated under reduced pressure
  4. dissolutionThe residue was redissolved in ethyl acetate
  5. washthe solution washed with water
  6. dry with materialthen dried over anhydrous magnesium sulfate
  7. filtrationThe solution was then filtered
  8. concentrationconcentrated under reduced pressure
  9. customThe residue was purified by column chromatography over silica eluting with hexane:acetone (3:1)

출처 및 근거

ORD 기록
ord-29f913015d1e467fabab1b28a67e44cd
출처 데이터셋
uspto-grants-2000_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06143751

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