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Water → 3-(3-Chlorophenyl)propionaldehyde

HRID 843573
ノート
印刷プレビュー

反応式

HRID 843573 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH:5]=[CH2:6].[CH2:10](Cl)Cl.[OH2:13]>FC(F)(F)C(O)=O>[Cl:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH2:5][CH2:6][CH:10]=[O:13]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 962WaterHCID 6344DichloromethaneHCID 14905m-Chlorostyrene

生成物 1

HCID 104195793-(3-Chlorophenyl)propionaldehyde

試薬・触媒・溶媒 1

HCID 6422Trifluoroacetic acid溶媒

実験手順

To a 25° C. solution of 3-chlorostyrene in anhydrous CH2Cl2 ( 10.0 g, 72.15 mmol) was added a well-stirred solution of Pb(OAc)4 (35.2 g, 79.4 mmol) in trifluoroacetic acid (150 mL), dropwise. Reaction was completed within 30 minutes of the addition and after being stirred for a further 30 minutes, the mixture was poured into water, extracted with ether (3×), the combined organic layers were washed with saturated NaHCO3 solution, water, dried (MgSO4), and concentrated to a volume of about 15 mL and immediately used for the following reaction described below.

後処理

  1. customReaction
  2. additionwas completed within 30 minutes of the addition
  3. extractionextracted with ether (3×)
  4. washthe combined organic layers were washed with saturated NaHCO3 solution, water
  5. dry with materialdried (MgSO4)
  6. concentrationconcentrated to a volume of about 15 mL
  7. customimmediately used for the following reaction

出典と根拠

ORDレコード
ord-80ae57e962354b54b94b849c380ee04b
出典データセット
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06380178B1

反応ノート

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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