HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl chloroformate → N-carbomethoxy-O-methylisourea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Carbamimidic acid, methyl ester, sulfate (1:1) | HCID 169039 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-carbomethoxy-O-methylisourea | HCID 53429793 | — |
Reaction Steps
To 52 parts of 2-methylpseudourea hydrogen sulfate in 250 parts of water at 0°-5° C. is added 31 parts of methyl chloroformate followed by dropwise addition of 74 parts of 50% sodium hydroxide. The reaction mass is stirred at room temperature for 3 hours and then extracted with methylene chloride. The methylene chloride extract is dried and the solvent evaporated. The residue is triturated with hexane to give 23 parts of methyl N-(1-amino-1-methoxy methylene)carbamate melting at 36°-39.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04121921 |
| Source dataset | uspto-grants-1978_10 |
| ORD ID | ord-c620b4aa2cb441edb5857353f5d62d2e |
| Source note | uspto-grants-1978_10 |