Hydrochloric Acid → N-tert-Butyl-N'-[2,6-di(butan-2-yl)phenyl]thiourea
Reaction equation
[CH:1]([C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([CH:11]([CH2:13][CH3:14])[CH3:12])[C:6]=1[N:15]=[C:16]=[S:17])([CH2:3][CH3:4])[CH3:2].Cl.[C:19]([NH2:23])([CH3:22])([CH3:21])[CH3:20]>>[CH:11]([C:7]1[CH:8]=[CH:9][CH:10]=[C:5]([CH:1]([CH2:3][CH3:4])[CH3:2])[C:6]=1[NH:15][C:16]([NH:23][C:19]([CH3:22])([CH3:21])[CH3:20])=[S:17])([CH2:13][CH3:14])[CH3:12]Participants
4
Procedure
20.6 g of 2,6-di-sec.-butyl-phenyl isothiocyanate are dissolved in 20.0 g of tert.-butylamine and the batch is kept for 12 hours at 20° C. It is then poured into dilute hydrochloric acid and the reaction product is filtered off, washed until neutral and dried.
Workup
- filtrationthe reaction product is filtered off
- washwashed until neutral and
- customdried
Sources & evidence
- ORD record
- ord-18d5863ac5624e8da7056b87cf03180f
- Source dataset
- uspto-grants-1980_03
- Patent number
- US04194008
Reaction notes
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