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HCID 22117812、化合物 → 1-(3-Bromo-4-chlorophenyl)ethan-1-one

HRID 1801610
ノート
印刷プレビュー

反応式

HRID 1801610 の反応式
[Br:1][C:2]1[CH:3]=[C:4]([CH:11]=[CH:12][C:13]=1[Cl:14])[C:5](N(OC)C)=[O:6].[CH3:15][Mg]Br>C1COCC1>[Br:1][C:2]1[CH:3]=[C:4]([C:5](=[O:6])[CH3:15])[CH:11]=[CH:12][C:13]=1[Cl:14]
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 22117812HCID 22117812、化合物HCID 178418573HCID 178418573、化合物

生成物 1

HCID 133472831-(3-Bromo-4-chlorophenyl)ethan-1-one収率 91%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
-5 °C

実験手順

A solution of 3-bromo-4-chloro-N-methoxy-N-methylbenzamide 105 (2.04 g, 7.3 mmol), was dissolved in 30 mL of dry THF. The solution was chilled to −5° C. in a salt bath under N2. Via syringe, methylmagnesium bromide (2.7 mL, 8.1 mmol) was added slowly to the solution. The solution was stirred for 2 h at −5° C., and then it was warmed to room temperature where it was stirred for another 1 h. The reaction was quenched with saturated NH4Cl, and it was diluted with ether and water. The organic solution was extracted with water and brine. The organic phase was dried over MgSO4, filtered, and concentrated in vacuo. The crude material was then filtered through a bed of silica and the filtrate was concentrated to give 1-(3-bromo-4-chlorophenyl)ethanone 106 (1.55 g, 91% yield) as a white solid.

後処理

  1. temperatureit was warmed to room temperature where it
  2. stirringwas stirred for another 1 h
  3. customThe reaction was quenched with saturated NH4Cl, and it
  4. additionwas diluted with ether and water
  5. extractionThe organic solution was extracted with water and brine
  6. dry with materialThe organic phase was dried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. filtrationThe crude material was then filtered through a bed of silica
  10. concentrationthe filtrate was concentrated

出典と根拠

ORDレコード
ord-1399b6cc26434366ac27f4cfcbf9358c
出典データセット
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08349831B2

反応ノート

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