Reaction equation
[Cl:1][C:2]1[C:7]([Cl:8])=[CH:6][CH:5]=[CH:4][C:3]=1[SH:9].[H-].[Na+].Cl[CH2:13][C:14]1[N:18]=[C:17]([CH3:19])[O:16][N:15]=1>O1CCCC1>[Cl:1][C:2]1[C:7]([Cl:8])=[CH:6][CH:5]=[CH:4][C:3]=1[S:9][CH2:13][C:14]1[N:18]=[C:17]([CH3:19])[O:16][N:15]=1Participants
Procedure
7.0 g (39.1 mmol) of 2,3-dichloro-thiophenol are introduced into 50 ml of absolute tetrahydrofuran, the mixture is treated with 1.2 g (0.039 mmol) of 80% sodium hydride dispersion in portions and stirred for 2 hours at reflux temperature. The mixture is subsequently treated with 4.5 g (33.9 mmol) of 3-chloromethyl-5-methyl-1,2,4-oxadiazole at room temperature and stirred until the reaction is complete (approximately 10 to 15 hours). The sodium chloride which has precipitated is subsequently separated off and the entire batch is concentrated in vacuo. The crude product which remains can be chromatographed over a silica gel column (silica gel 60-Merck, particle size: 0.040 to 0.063 mm) using toluene as the eluent. 3.8 g (36.5% of theory) of 3-(2,3-dichlorophenylthiomethyl)-5-methyl-1,2,4-oxadiazole are obtained.
Workup
- temperatureat reflux temperature
- stirringstirred until the reaction
- custom(approximately 10 to 15 hours)
- customThe sodium chloride which has precipitated
- customis subsequently separated off
- concentrationthe entire batch is concentrated in vacuo
- customThe crude product which remains can be chromatographed over a silica gel column (silica gel 60-Merck, particle size: 0.040 to 0.063 mm)
Sources & evidence
- ORD record
- ord-bfc60d7b03054bb0bd5938345113d8c0
- Source dataset
- uspto-grants-1995_06
- Patent number
- US05428047
Linked notes
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