4-Chlorophenyl isothiocyanate → HCID 178444017, compound
Reaction equation
[Na].Cl.[CH3:3][C:4]([CH3:11])([CH3:10])[CH2:5][CH2:6][C:7]([NH2:9])=[NH:8].[Cl:12][C:13]1[CH:18]=[CH:17][C:16]([N:19]=[C:20]=[S:21])=[CH:15][CH:14]=1>CC(C)=O>[Cl:12][C:13]1[CH:18]=[CH:17][C:16]([NH:19][C:20]([NH:8][C:7](=[NH:9])[CH2:6][CH2:5][C:4]([CH3:11])([CH3:10])[CH3:3])=[S:21])=[CH:15][CH:14]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Following a procedure similar to that described in Example 42 but using 7.22 g. sodium in 705 ml. dry acetone, 51.7 g. 4,4-dimethylvaleramidine hydrochloride, and 53.2 g. 4-chlorophenyl isothiocyanate in 350 ml. dry acetone there was obtained 1-(4-chlorophenyl)-3-(4,4-dimethylpentanimidoyl)-2-thiourea; m.p. 135°-137°C. (from acetonitrile); hydrochloride (80.7 g.), m.p. 182°-186°C.
Sources & evidence
- ORD record
- ord-6af99b01ff1848ca8f11c9a608a4e0b0
- Source dataset
- uspto-grants-1976_10
- Patent number
- US03984467
Reaction notes
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