Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Calcium Hydroxide | HCID 6093208 | — |
| Reactant | HCID 86738943 | HCID 86738943 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13755316 | HCID 13755316 | — |
Reaction Steps
14.1 g of alpha-chloro-beta-aminopropionitrile hydrochloride was dissolved in 160 g of water, and with stirring, 12 g of calcium hydroxide was gradually added. Then, the reaction mixture was heated to 60° C., and reacted at 60° to 65° C. for 8 hours. After the reaction, the excess of calcium hydroxide was removed by filtration. The residue was analyzed by high-speed liquid chromatography in the same way as in Example 1. The yield of calcium aziridine-2-carboxylate formed was 92.5%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04393000 |
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| Source dataset | uspto-grants-1983_07 |
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| ORD ID | ord-9d2139bdf5e64982bff0adc504f4e0aa |
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| Source note | uspto-grants-1983_07 |
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