Hydrochloric Acid → HCID 21556724, compound
Reaction equation
[CH3:1][O:2][C:3](=[O:7])[CH2:4][C:5]#[N:6].[CH2:8]([CH:10]1[O:12]C1)[Cl:9].Cl>>[ClH:9].[CH3:1][O:2][C:3]([CH2:4][C:5](=[NH:6])[O:12][CH2:10][CH2:8][Cl:9])=[O:7]Participants
4
Procedure
A mixture of 9.9 parts of methylcyanoacetate and 8.05 parts of epichlorohydrin was saturated with dry hydrogen chloride gas under ice-cooling and further cooled with icewater for one hour, followed by keeping in a refrigerator overnight. The resulting solid was washed with ethylether and dried to give 19.9 parts of 2-chloroethyl methoxycarbonylacetimidate hydrochloride. Yield 92% Melting point: 103 to 107°C (decomposition).
Workup
- temperaturecooling
- temperaturefurther cooled with icewater for one hour
- customby keeping in a refrigerator overnight
- washThe resulting solid was washed with ethylether
- customdried
Sources & evidence
- ORD record
- ord-6d88278e1412400186fba47fc52c059b
- Source dataset
- uspto-grants-1976_03
- Patent number
- US03941823
Reaction notes
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