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Dimethylformamide → 2-(4-Methoxy-2,3-dimethylphenyl)-1-(pyrrolidin-1-yl)ethanone

HRID 2423285
ノート
印刷プレビュー

反応式

HRID 2423285 の反応式
Br[C:2](Br)=[CH:3][C:4]1[CH:9]=[CH:8][C:7]([O:10][CH3:11])=[C:6]([CH3:12])[C:5]=1[CH3:13].[NH:15]1[CH2:19][CH2:18][CH2:17][CH2:16]1.CN(C=[O:24])C>O.CCOCC>[CH3:11][O:10][C:7]1[CH:8]=[CH:9][C:4]([CH2:3][C:2]([N:15]2[CH2:19][CH2:18][CH2:17][CH2:16]2)=[O:24])=[C:5]([CH3:13])[C:6]=1[CH3:12]
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 6228DimethylformamideHCID 31268PyrrolidineHCID 59864791HCID 59864791、化合物

生成物 1

HCID 598648482-(4-Methoxy-2,3-dimethylphenyl)-1-(pyrrolidin-1-yl)ethanone

試薬・触媒・溶媒 2

HCID 962Water溶媒2 回HCID 3283Diethyl Ether溶媒

反応条件

温度
80 °C

実験手順

Under an N2 atmosphere, 1-(2,2-dibromovinyl)-4-methoxy-2,3-dimethylbenzene was dissolved in a mixture of DMF (43 mL) and water (14 mL). Pyrrolidine (5.67 mL, 68 mmol) was added and the reaction was heated to 80° C. for 20 h. The reaction was diluted with Et2O and water. The layers were separated and the organic layer was washed with 0.25M HCl (aq) and brine. The organic extract was dried (Na2SO4), filtered, and concentrated in vacuo. Flash column chromatography of the residue, eluting with 0% to 100% ethyl acetate in hexanes, afforded the title compound. LC-MS ESI (pos.) m/z: 248.2 (M+H).

後処理

  1. customThe layers were separated
  2. washthe organic layer was washed with 0.25M HCl (aq) and brine
  3. extractionThe organic extract
  4. dry with materialwas dried (Na2SO4)
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. washFlash column chromatography of the residue, eluting with 0% to 100% ethyl acetate in hexanes

出典と根拠

ORDレコード
ord-ff444e80e37843a2800e226d1dabe5dd
出典データセット
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07960567B2

反応ノート

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