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Acetone → HCID 59655945、化合物

HRID 2054451
ノート
印刷プレビュー

反応式

HRID 2054451 の反応式
[CH3:1][C:2]([CH3:4])=O.S(=O)(=O)(O)O.[Br:10][C:11]1[CH:17]=[C:16]([CH3:18])[C:15]([CH3:19])=[CH:14][C:12]=1[NH2:13].[BH4-].[Na+]>O1CCCC1>[Br:10][C:11]1[CH:17]=[C:16]([CH3:18])[C:15]([CH3:19])=[CH:14][C:12]=1[NH:13][CH:2]([CH3:4])[CH3:1]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 180AcetoneHCID 1118Sulfuric AcidHCID 41792362-bromo-4,5-dimethylanilineHCID 4311764Sodium borohydride

生成物 1

HCID 59655945HCID 59655945、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

A solution of acetone (5.60 mL, 76.3 mmol) and aqueous 4 M sulfuric acid (5.20 mL, 20.8 mmol) in tetrahydrofuran (15 mL) was added dropwise to a stirred solution of 2-bromo-4,5-dimethylaniline 1-8 (13.9 g, 69.3 mmol) in tetrahydrofuran (40 mL) at approximately 0° C. Sodium borohydride (2.62 g, 69.3 mmol) was added cautiously and the resulting mixture allowed to warm to ambient temperature. After 30 min, the reaction was quenched by the careful sequential addition of water (25 mL) and sodium hydroxide pellets (until strongly alkaline). The reaction mixture was extracted with tert-butyl methyl ether (150 mL) and the organic phase was washed with brine, dried (sodium sulfate) and concentrated in vacuo to give a crude residue. Purification of the crude residue by flash chromatography over silica gel (gradient elution; 0%-20% ethyl acetate/hexanes as eluent) afforded 1-9 as a clear, pale orange oil.

後処理

  1. customthe reaction was quenched by the careful sequential addition of water (25 mL) and sodium hydroxide pellets (until strongly alkaline)
  2. extractionThe reaction mixture was extracted with tert-butyl methyl ether (150 mL)
  3. washthe organic phase was washed with brine
  4. dry with materialdried (sodium sulfate)
  5. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-c17a7f77ff3242d6838155ea91ff6892
出典データセット
uspto-grants-2008_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07329673B2

反応ノート

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