HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 866718Generated: October 31, 2026
Dimethyl Sulfate → Carbamic acid, cyanomethyl-, ethyl ester
https://huagongshe.com/reaction/866718
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Cyanamide | HCID 9864 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Water | HCID 962 | — |
| Product | Carbamic acid, cyanomethyl-, ethyl ester | HCID 109009 | 81% |
Reaction Steps
657 Parts of ethyl chloroformate and 945 parts of a 50% aqueous sodium hydroxide solution were added simultaneously to a solution of 504 parts of a 50% aqueous cyanamide solution in 825 parts of water at 25° during a period of 90 minutes and at a pH of 6.9 to 7.1. As the addition of the reactants progressed, the temperature of the reaction mass was allowed to rise to 53°-55° and was maintained within that range by cooling. When the addition was complete, the reaction mass was cooled to 40°. Dimethylsulfate (1,134 parts) was then added during one hour with stirring while maintaining the pH at 7 to 7.1 by the addition of 50% aqueous sodium hydroxide solution. After holding 3 hours at 40° the resulting two-phase solution was transferred to a separatory funnel. The upper phase of N-ethoxycarbonyl-N-methylcyanamide was separated and the lower aqueous phase was sent to secondary recovery, either distillation or extraction. The upper phase of 669 parts was 93% N-ethoxycarbonyl-N-methylcyanamide (81% yield). This upper phase is usually pure enough for subsequent steps. However, vacuum distillation was used to provide pure N-ethoxycarbonyl-N-methylcyanamide, b.p. 67° at 2.2 mm.Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04101308 |
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| Source dataset | uspto-grants-1978_07 |
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| ORD ID | ord-5a70e3ec42e04d3aaa5ec77584fb30f3 |
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| Source note | uspto-grants-1978_07 |
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