Carbonic acid-guanidine (1:1) → HCID 22150373, compound
Reaction equation
C(=O)(O)O.[NH2:5][C:6]([NH2:8])=[NH:7].CN([CH:12]=[CH:13][C:14]([C:16]1[CH:21]=[CH:20][C:19]([C:22]([CH3:25])([CH3:24])[CH3:23])=[CH:18][CH:17]=1)=O)C>C(O)C>[NH2:7][C:6]1[N:8]=[C:14]([C:16]2[CH:17]=[CH:18][C:19]([C:22]([CH3:25])([CH3:24])[CH3:23])=[CH:20][CH:21]=2)[CH:13]=[CH:12][N:5]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Sodium metal (10.4 g) was added to absolute ethanol (40 ml). When all the sodium had dissolved, the sodium ethoxide solution so formed was added to a mixture of guanidine carbonate (1.56 g) and (1-(N,N-dimethylamino)-3-(4-(1,1-dimethylethyl) phenyl)prop-1-en-3-one (2.5 g) dissolved in absolute ethanol (40 ml) and the mixture heated under reflux with stirring overnight. The reaction was followed by tlc. On cooling the solid material formed was filtered and washed with water to remove Na2CO3 to give a white crystalline solid, m.p. 186° C.
Workup
- temperaturethe mixture heated
- temperatureunder reflux
- temperatureOn cooling the solid material
- customformed
- filtrationwas filtered
- washwashed with water
- customto remove Na2CO3
- customto give a white crystalline solid, m.p. 186° C.
Sources & evidence
- ORD record
- ord-9f4924f3dec84cd2a6e1669d77bf73c2
- Source dataset
- uspto-grants-1991_01
- Patent number
- US04983619
Reaction notes
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