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Hydrochloric Acid → 3-Bromo-4-chlorobenzaldehyde

HRID 1275839
ノート
印刷プレビュー

反応式

HRID 1275839 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].[H-].[Al+3].[Li+].[H-].[H-].[H-].[Cl-].[NH4+].Cl>O1CCCC1>[Br:1][C:2]1[CH:3]=[C:4]([CH:11]=[CH:12][C:13]=1[Cl:14])[CH:5]=[O:6]
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 313Hydrochloric AcidHCID 25517Ammonium ChlorideHCID 21226445Aluminium lithium hydrideHCID 22117812HCID 22117812、化合物

生成物 1

HCID 140498093-Bromo-4-chlorobenzaldehyde収率 80.7%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回
このページの内容参加物実験手順後処理出典と根拠反応ノート

実験手順

A solution of 10.7 g of 3-bromo-4-chloro-N-methoxy-N-methylbenzamide in 100 ml of anhydrous tetrahydrofuran was added dropwise to 43 ml of a 1M solution of lithium aluminium hydride in tetrahydrofuran at below 5° C., and stirred for 1 hour. 100 ml of saturated ammonium chloride solution was then added cautiously followed by 100 ml of a 1M solution of hydrochloric acid and the mixture was extracted twice with 400 ml of diethyl ether. The combined organic extracts were dried over anhydrous sodium sulphate and concentrated under reduced pressure to give 6.8 g of 3-bromo-4-chlorobenzaldehyde as a pale yellow solid.

後処理

  1. extractionthe mixture was extracted twice with 400 ml of diethyl ether
  2. dry with materialThe combined organic extracts were dried over anhydrous sodium sulphate
  3. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-814a2a4b25a74e638e6b5a855f76014b
出典データセット
uspto-grants-2000_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06162918

反応ノート

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