Diethyl Ether → HCID 14705803, compound
Reaction equation
[C:1]([S:20]/[CH:21]=[CH:22]\[C:23]1[CH:24]=[N:25][CH:26]=[CH:27][CH:28]=1)([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C[I:30].[CH2:31](OCC)C>C(Cl)Cl>[I-:30].[C:1]([S:20]/[CH:21]=[CH:22]\[C:23]1[CH:24]=[N+:25]([CH3:31])[CH:26]=[CH:27][CH:28]=1)([C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1)([C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 3-[(Z)-2-(tritylthio)vinyl]pyridine (5 g) and methyl iodide (8.3 ml) in dry methylene chloride (100 ml) was stirred at ambient temperature for 24 hours. The reaction mixture was poured into diethyl ether under stirring. The resultant precipitate was collected by filtration, washed with diethyl ether and air-dried at ambient temperature to give 3-[(Z)-2-(tritylthio)vinyl]-1-methylpyridinium iodide (6.64 g) as yellow powder.
Workup
- stirringunder stirring
- filtrationThe resultant precipitate was collected by filtration
- washwashed with diethyl ether
- customair-dried at ambient temperature
Sources & evidence
- ORD record
- ord-acd36d227d9147bb8e878e03d412e4b4
- Source dataset
- uspto-grants-1986_11
- Patent number
- US04622318
Reaction notes
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