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Chloromethyl Methyl Ether → HCID 23116091, Verbindung

HRID 1174047
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1174047
[CH:1]([N:4]1[CH2:8][CH2:7][CH2:6][CH2:5]1)([CH3:3])[CH3:2].[CH3:9][O:10][CH2:11][Cl:12]>CC(=O)CC>[Cl-:12].[CH3:9][O:10][CH2:11][N+:4]1([CH:1]([CH3:3])[CH3:2])[CH2:8][CH2:7][CH2:6][CH2:5]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 7864Chloromethyl Methyl EtherHCID 124163241-(Propan-2-yl)pyrrolidine

Produkt 1

HCID 23116091HCID 23116091, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6569Methyl Ethyl KetoneLösungsmittel

Versuchsvorschrift

A 40.00 g quantity of N-isopropylpyrrolidine was dissolved in 361 g of dehydrated 2-butanone (reagent, product of Wako Pure Chemical Ind. Ltd.), followed by replacement with nitrogen. To the solution was added dropwise 28.76 g of chloromethyl methyl ether (reagent, product of Tokyo Kasei Co., Ltd. as purified by distillation) at 5° C. over a period of 0.5 hour. The mixture was thereafter heated to a gradually elevated temperature and stirred at room temperature for 10 hours, whereby the reaction was terminated. The reaction mixture was cooled to 5° C., and the resulting solids were filtered off in nitrogen. The filter cake was washed with 200 ml of 2-butanone and thereafter dried in a vacuum, giving 66.40 g of the desired product.

Aufarbeitung

  1. temperatureThe mixture was thereafter heated to a gradually elevated temperature
  2. customwhereby the reaction was terminated
  3. temperatureThe reaction mixture was cooled to 5° C.
  4. filtrationthe resulting solids were filtered off in nitrogen
  5. washThe filter cake was washed with 200 ml of 2-butanone
  6. customdried in a vacuum

Quellen und Nachweise

ORD-Eintrag
ord-672b282b7418435eb7f10575007d1fe4
Quelldatensatz
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07834197B2

Notizen zur Reaktion

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