Butyl isocyanate → HCID 152748181, compound
Reaction equation
[Na].Cl.[C:3]([NH2:11])(=[NH:10])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[CH2:12]([N:16]=[C:17]=[O:18])[CH2:13][CH2:14][CH3:15]>CC(C)=O>[CH2:12]([NH:16][C:17]([NH:10][C:3](=[NH:11])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)=[O:18])[CH2:13][CH2:14][CH3:15]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Following a procedure similar to that described in Example 23 but using 7.7 g. sodium in 1100 ml. dry sodium, 52.4 g. benzamidine hydrochloride, and 33.1 g. butylisocyanate in 400 ml. dry acetone there was obtained, after recrystallization from ethyl acetate, 62.2 g. 1-butyl-3-(benzimidoyl)urea hydrochloride; m.p. 139°-141°C.
Workup
- customafter recrystallization from ethyl acetate, 62.2 g
Sources & evidence
- ORD record
- ord-4cf6b54dfb5d4e788e781efd6f02028a
- Source dataset
- uspto-grants-1976_10
- Patent number
- US03984467
Reaction notes
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