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Tri-tert-butylphosphine tetrafluoroborate → 6-(1,3-Dioxolan-2-ylmethyl)-3,4-dihydroisochromen-1-one

HRID 1466114
ノート
印刷プレビュー

反応式

HRID 1466114 の反応式
Br[C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C:8](=[O:12])[O:7][CH2:6][CH2:5]2.F[B-](F)(F)F.C([PH+](C(C)(C)C)C(C)(C)C)(C)(C)C.Br[Zn][CH2:33][CH:34]1[O:38][CH2:37][CH2:36][O:35]1>CN(C=O)C.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[O:35]1[CH2:36][CH2:37][O:38][CH:34]1[CH2:33][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C:8](=[O:12])[O:7][CH2:6][CH2:5]2
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 2734635Tri-tert-butylphosphine tetrafluoroborateHCID 441308436-bromo-3,4-dihydro-1H-2-benzopyran-1-oneHCID 178419777HCID 178419777、化合物

生成物 1

HCID 675173746-(1,3-Dioxolan-2-ylmethyl)-3,4-dihydroisochromen-1-one

試薬・触媒・溶媒 2

HCID 167845palladium(II) acetate触媒
HCID 6228
Dimethylformamide
溶媒

反応条件

温度
85 °C

実験手順

6-bromo-3,4-dihydro-1H-isochromen-1-one (10 g, 44 mmol) was combined with tri-t-butyl phosphonium tetrafluoroborate (256 mg, 0.881 mmol), palladium (II) acetate (99 mg, 0.44 mmol) and commercially available bromo(1,3-dioxolan-2-ylmethyl)zinc solution (0.5 M, 97 mL, 48 mmol) in DMF (100 mL), and the mixture was degassed three times by alternating vacuum and nitrogen purge. The mixture was then heated at 85° C. for 6 h, then was stirred at RT overnight. Ethyl acetate and ether were added and the mixture was washed with water. The aqueous layer was extracted with ethyl acetate, the organic layers were combined, and washed twice with water and once with brine. The organic layer was dried over MgSO4, filtered and concentrated. The crude product was purified by MPLC (silica) eluting with ethyl acetate in hexanes to afford the title compound. LCMS: m/z 235 (M+1)+.

後処理

  1. customthe mixture was degassed three times
  2. custompurge
  3. additionEthyl acetate and ether were added
  4. washthe mixture was washed with water
  5. extractionThe aqueous layer was extracted with ethyl acetate
  6. washwashed twice with water and once with brine
  7. dry with materialThe organic layer was dried over MgSO4
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customThe crude product was purified by MPLC (silica)
  11. washeluting with ethyl acetate in hexanes

出典と根拠

ORDレコード
ord-5cb41f3a357142578481943aedb1d0e3
出典データセット
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08999990B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート