N-bromobutanimide → HCID 19940138、化合物

HRID 974351ノート

反応式

HRID 974351 の反応式
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]1[NH:7][C:8]([C:11]2[S:12][CH:13]=[CH:14][CH:15]=2)=[CH:9][CH:10]=1.[Br:16]N1C(=O)CCC1=O>O1CCCC1>[Br:16][C:9]1[CH:10]=[C:6]([C:2]2[S:1][CH:5]=[CH:4][CH:3]=2)[NH:7][C:8]=1[C:11]1[S:12][CH:13]=[CH:14][CH:15]=1

参加物

4

反応物 2

HCID 67184N-bromobutanimideHCID 41751102,5-Di(thiophen-2-yl)-1H-pyrrole

生成物 1

HCID 19940138HCID 19940138、化合物収率 46.6%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of 2,5-dithienylpyrrole (130 mg, 0.56 mmol) in 2.5 mL of anhydrous tetrahydrofuran cooled to -78° C. was added N-bromosuccinimide (99.68 mg, 0.56 mmol). After addition was complete the cooling bath was removed and the reaction mixture was allowed to stand in a -20° C. freezer for 4 hours, during which the solution became a brown color. The reaction mixture was concentrated under reduced pressure, carbon tetrachloride was added to precipitate the succinimide, and this mixture was filtered. The filter cake was washed with additional chloroform, the combined filtrates were concentrated, and the resulting oil was chromatographed on silica gel (50 g). Elution with hexane-ethyl acetate, 4:1, furnished 81 mg (46%) of 3-bromo-2,5-dithienylpyrrole.

後処理

  1. additionAfter addition
  2. customwas removed
  3. concentrationThe reaction mixture was concentrated under reduced pressure, carbon tetrachloride
  4. additionwas added
  5. customto precipitate the succinimide
  6. filtrationthis mixture was filtered
  7. washThe filter cake was washed with additional chloroform
  8. concentrationthe combined filtrates were concentrated
  9. customthe resulting oil was chromatographed on silica gel (50 g)
  10. washElution with hexane-ethyl acetate, 4:1

出典と根拠

ORDレコード
ord-c09e22c97d954a0889595db302d70d19
出典データセット
uspto-grants-1991_11
特許番号
US05068355

反応ノート

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