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Dichloromethane → HCID 17764601, Verbindung

HRID 2121720
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2121720
[Cl:1][C:2]1[S:3][C:4](Cl)=[CH:5][C:6]=1[CH3:7].C[O:10]C(Cl)Cl.[CH2:14]([Cl:16])Cl>Cl[Ti](Cl)(Cl)Cl>[Cl:1][C:2]1[S:3][C:14]([Cl:16])=[C:5]([CH3:4])[C:6]=1[CH:7]=[O:10]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 6344DichloromethaneHCID 21004Methane, dichloromethoxy-HCID 2689102,5-Dichloro-3-methylthiophene

Produkt 1

HCID 17764601HCID 17764601, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 24193Titanium TetrachlorideKatalysator

Versuchsvorschrift

To a stirred solution of 2,5-dichloro-3-methylthiophene [prepared according to the method of J. Amer. Chim. Soc., 1971, 333.] (11.8 g) in CH2Cl2 (200 mL) was added TiCl4(37.94 g) and dichloromethyl methyl ether (12.6 g) at −10° C. After stirring for 4 hours, the reaction mixture was poured into ice-water and the whole was stirred vigorously for 30 minutes. The resulting mixture was extracted with CH2Cl2 (200 ml×1), and the organic layers was washed with saturated NaHCO3 solution(100 mL×1), brine (100 mL×1), dried over MgSO4, and concentrated in vacuo. The resulting residue was purified by distillation (bp: 140-145° C./10 mmHg) to provide the subtitle compound (11.75 g).

Aufarbeitung

  1. stirringthe whole was stirred vigorously for 30 minutes
  2. extractionThe resulting mixture was extracted with CH2Cl2 (200 ml×1)
  3. washthe organic layers was washed with saturated NaHCO3 solution(100 mL×1), brine (100 mL×1)
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated in vacuo
  6. distillationThe resulting residue was purified by distillation (bp: 140-145° C./10 mmHg)

Quellen und Nachweise

ORD-Eintrag
ord-0129fc2a09e44cd0b01f620e7a67df42
Quelldatensatz
uspto-grants-2004_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06696470B2

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