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Acetic Acid → 6-Bromo-3,4-dihydro-4-methyl-2(1H)-quinoxalinone

HRID 2358967
ノート
印刷プレビュー

反応式

HRID 2358967 の反応式
[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[NH:8][C:7](=[O:12])[CH2:6][NH:5]2.C=O.O.[C:16](O)(=O)C.[BH3-]C#N.[Na+]>CO>[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[NH:8][C:7](=[O:12])[CH2:6][N:5]2[CH3:16]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 176Acetic AcidHCID 712FormaldehydeHCID 962WaterHCID 5003444Sodium cyanoborohydrideHCID 669113076-Bromo-1,2,3,4-tetrahydroquinoxalin-2-one

生成物 1

HCID 226677406-Bromo-3,4-dihydro-4-methyl-2(1H)-quinoxalinone収率 94%

試薬・触媒・溶媒 1

HCID 887
Methanol
溶媒

実験手順

To a solution of 6-bromo-3,4-dihydroquinoxalin-2(1H)-one (370 mg, 1.63 mmol) in 10 ml methanol was added a solution of 37% formaldehyde in water (59 mg, 1.95 mmol) and acetic acid (196 mg, 3.26 mmol). The mixture was stirred at room temperature for 2 h, then refluxed for 1 h. After addition of NaBH3CN (307 mg, 4.89 mmol) stirring was continued for 2.5 h at room temperature. Then methanol was removed under vacuum. To the remaining mixture water was added. Then the solution was basified to pH 8-9 with an aqueous solution of sodium hydrogen carbonate and extracted several times with ethyl acetate. The combined organic layers were washed with brine, dried over MgSO4 and evaporated, affording 6-bromo-4-methyl-3,4-dihydroquinoxalin-2(1H)-one (369 mg, 1.53 mmol, 94%) as off-white solid.

後処理

  1. temperaturerefluxed for 1 h
  2. stirringstirring
  3. waitwas continued for 2.5 h at room temperature
  4. customThen methanol was removed under vacuum
  5. additionTo the remaining mixture water was added
  6. extractionextracted several times with ethyl acetate
  7. washThe combined organic layers were washed with brine
  8. dry with materialdried over MgSO4
  9. customevaporated

出典と根拠

ORDレコード
ord-f9175441841f47ea800a8ab9c4b3cc3a
出典データセット
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08685960B2

反応ノート

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