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Water → 3-(3-Chlorophenyl)propionaldehyde

HRID 843573
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 843573
[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]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 962WaterHCID 6344DichloromethaneHCID 14905m-Chlorostyrene

Produkt 1

HCID 104195793-(3-Chlorophenyl)propionaldehyde

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6422Trifluoroacetic acidLösungsmittel

Versuchsvorschrift

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.

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Aufarbeitung

  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

Quellen und Nachweise

ORD-Eintrag
ord-80ae57e962354b54b94b849c380ee04b
Quelldatensatz
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06380178B1

Notizen zur Reaktion

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