HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418707Generated: October 25, 2026
Ethyl chloroformate → Carbamic acid, N-(cyanomethyl)-, ethyl ester
https://huagongshe.com/reaction/1418707
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aminoacetonitrile sulfate (1:1) | HCID 196971 | — |
| Solvent | Water | HCID 962 | — |
| Product | Carbamic acid, N-(cyanomethyl)-, ethyl ester | HCID 83704 | 97% |
Reaction Steps
Aminoacetonitrile sulfate (H2NCH2CN.1/2H2SO4, 121.5 g, 1.156mole) was dissolved in water (230.9 g) and the solution was cooled to 0° to 5° C. and adjusted to pH 5 to 7 by the addition of a small amount of 30% aqueous sodium hydroxide solution. Ethyl chloroformate (108.5 g, 1.00 mole) and 30% aqueous sodium hydroxide solution were concurrently added dropwise with stirring and keeping pH at 5 to 7 at 0° to 5° C. over 2 hours and the mixture was stirred at the same temperature for additional 2 hours while keeping the same pH by dropping, if necessary, 30% aqueous sodium hydroxide solution. The total amount of 30% aqueous sodium hydroxide solution was 294.3 g. The reaction mixture was extracted three times with toluene (485 ml). The toluene layer was dried over anhydrous magnesium sulfate, toluene was evaporated and the residue was cooled to room temperature to give crystals (124.7 g, 0.968 mole) of ethyl N-cyanomethylcarbamate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05883260 |
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| Source dataset | uspto-grants-1999_03 |
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| ORD ID | ord-497022630c1f4e958d92caf3f54fefa2 |
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| Source note | uspto-grants-1999_03 |
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