Dimethyl Sulfate → Carbamic acid, cyanomethyl-, ethyl ester

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.

1. additionAs the addition of the reactants
2. customto rise to 53°-55°
3. temperaturewas maintained within that range
4. temperatureby cooling
5. additionWhen the addition
6. temperaturethe reaction mass was cooled to 40°
7. temperaturewhile maintaining the pH at 7 to 7.1
8. customthe resulting two-phase solution was transferred to a separatory funnel
9. customThe upper phase of N-ethoxycarbonyl-N-methylcyanamide was separated
10. distillationthe lower aqueous phase was sent to secondary recovery, either distillation or extraction

ORD record

ord-26a540a6087c4d4c9aa13a0b03ab338e

Source dataset

uspto-grants-1978_01

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US04069037