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Bromine → HCID 15257067、化合物

HRID 589047
ノート
印刷プレビュー

反応式

HRID 589047 の反応式
[Br:1]Br.[CH3:3][CH:4]([CH3:13])[C:5]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][N:8]=1)=[O:6]>C(O)(=O)C>[Br:1][C:4]([CH3:13])([CH3:3])[C:5]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][N:8]=1)=[O:6]
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

4

反応物 2

HCID 24408BromineHCID 101083Isopropyl 2-pyridyl ketone

生成物 1

HCID 15257067HCID 15257067、化合物

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒2 回

反応条件

温度
105 °C

実験手順

Bromine (2.1 g, 13.4 mmol) dissolved in acetic acid (1 mL) was added slowly to a mixture of 2-methyl-(1-pyridin-2-yl)propan-1-one (2.0 g, 13 mmol) in acetic acid (20 mL) at room temperature. The reaction was heated to 105° C. for 3 h, allowed to cool to room temperature, and concentrated in vacuo to give a dark semisolid. The crude product was partitioned between ethyl acetate and saturated aqueous sodium bicarbonate. The combined organic layer was washed with brine, dried over magnesium sulfate, and concentrated to give 2-bromo-2-methyl-1-(pyridin-2-yl)propan-1-one as a very dark oil (3.0 g, 98%). LCMS calculated for C9H11BrNO (M+H)+: m/z=227.9, 229.9. found: 228.1, 230.1.

後処理

  1. temperatureto cool to room temperature
  2. concentrationconcentrated in vacuo
  3. customto give a dark semisolid
  4. customThe crude product was partitioned between ethyl acetate and saturated aqueous sodium bicarbonate
  5. washThe combined organic layer was washed with brine
  6. dry with materialdried over magnesium sulfate
  7. concentrationconcentrated

出典と根拠

ORDレコード
ord-f2a6d89a5a294974a64d40c81ed4dd49
出典データセット
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09227985B2

反応ノート

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