Pyridinium, 1-(2-ethoxy-2-oxoethyl)-, bromide (1:1) → N-(Ethoxycarbonylmethyl)pyridinium Tetraphenylborate

HRID 1614295Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1614295
[Br-].[CH2:2]([O:4][C:5]([CH2:7][N+:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)=[O:6])[CH3:3].[C:14]1([B-:20]([C:33]2[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=2)([C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=2)[C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.[Na+]>O>[C:33]1([B-:20]([C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=2)([C:21]2[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=2)[C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=2)[CH:34]=[CH:35][CH:36]=[CH:37][CH:38]=1.[CH2:2]([O:4][C:5]([CH2:7][N+:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)=[O:6])[CH3:3]

Komponenten

4

Versuchsvorschrift

To a solution of 24.61 grams (0.10 mol) of N-(ethoxycarbonylmethyl)pyridinium bromide in 100 milliliters of water, there was added a solution of 34.22 grams (0.10 mol) of sodium tetraphenylborate in 150 milliliters of water. The mixture was diluted with 1 liter of water and filtered. The solid collected was dissolved in methylene chloride, the water layer was separated and the organic layer was dried over MgSO4 and concentrated. Recrystallization from ethyl acetate yielded 21.9 grams of product (45.11% of theory); mp=150°-152° C.

Aufarbeitung

  1. filtrationfiltered
  2. customThe solid collected
  3. dissolutionwas dissolved in methylene chloride
  4. customthe water layer was separated
  5. dry with materialthe organic layer was dried over MgSO4
  6. concentrationconcentrated
  7. customRecrystallization from ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-1d4248cf4eca48c7a5a478a6817b58e0
Quelldatensatz
uspto-grants-1993_03
Patentnummer
US05196538

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