Cyanamide → HCID 12272861, compound
Reaction equation
Cl.[C:2]([CH2:4][C:5](=[NH:8])[O:6][CH3:7])#[N:3].[N:9]#[C:10]N>C1C=CC=CC=1>[C:10]([N:8]=[C:5]([O:6][CH3:7])[CH2:4][C:2]#[N:3])#[N:9]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
2.69 g of methyl cyanoacetimidate hydrochloride, 1.68 g of cyanamide and 5.0 g of molecular sieve (type 4A, 60 mesh through) were suspended in 30 ml of benzene and the suspension was made to react for 5 hours at 25°C under stirring. After reaction, insoluble materials were filtered off and then the filtrate was concentrated to dryness in vacuo to give 2.26 g of methyl N-cyanocyanoacetimidate (yield 91.2%) mp 45.5°C.
Workup
- customto react for 5 hours at 25°C
- customAfter reaction, insoluble materials
- filtrationwere filtered off
- concentrationthe filtrate was concentrated to dryness in vacuo
Sources & evidence
- ORD record
- ord-02cb4942e9414deb8c69533af79c931b
- Source dataset
- uspto-grants-1976_04
- Patent number
- US03948915
Reaction notes
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