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1,3-Propanediol → 2,2-dimethyl-2H-pyrano[2,3-g]quinoline

HRID 2425365
ノート
印刷プレビュー

反応式

HRID 2425365 の反応式
[NH2:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[O:8][C:7]([CH3:13])([CH3:12])[CH:6]=[CH:5]2.[CH2:14](O)[CH2:15][CH2:16]O.C(P(CCCC)CCCC)CCC>COCCOC.[Ru](Cl)(Cl)Cl>[CH3:12][C:7]1([CH3:13])[O:8][C:9]2=[CH:10][C:11]3[CH:14]=[CH:15][CH:16]=[N:1][C:2]=3[CH:3]=[C:4]2[CH:5]=[CH:6]1
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 104421,3-PropanediolHCID 13831TributylphosphineHCID 100808812,2-Dimethyl-2H-chromen-6-amine

生成物 1

HCID 591344202,2-dimethyl-2H-pyrano[2,3-g]quinoline収率 59%

試薬・触媒・溶媒 2

HCID 61850Ruthenium trichloride触媒HCID 80711,2-Dimethoxyethane
溶媒

反応条件

温度
180 °C

実験手順

Under nitrogen atmosphere, to a solution of 6-amino-2,2-dimethylchromene (3.88 g, 22.1 mmol) and ruthenium trichloride (55.0 mg, 0.265 mmol) in dimethylene glycol dimethyl ether (8 mL), 1,3-propanediol (0.639 mL, 8.84 mmol) and tri-n-butyl phosphine (0.132 mL, 0.530 mmol) were added at room temperature, and the resulting mixture was stirred at 180° C. for 5 hours. Upon the completion of the reaction, ruthenium complex was removed by florisil column, and solvent was distilled off. The residue was purified by medium pressure column chromatography (hexane/ethyl acetate=5/1) and the aimed product was obtained (yield: 59%).

後処理

  1. customUpon the completion of the reaction, ruthenium complex
  2. customwas removed by florisil column, and solvent
  3. distillationwas distilled off
  4. customThe residue was purified by medium pressure column chromatography (hexane/ethyl acetate=5/1)

出典と根拠

ORDレコード
ord-4d7e4c30726541d6837b3dc08d988bbb
出典データセット
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07964623B2

反応ノート

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