HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25917Generated: October 25, 2026
1-Bromopropane → 2-[N-(2-cyanoethyl)anilino]ethyl N-propylcarbamate
https://huagongshe.com/reaction/25917
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromopropane | HCID 7840 | — |
| Reactant | Sulfolane | HCID 31347 | — |
| Reactant | Propanenitrile, 3-[(2-hydroxyethyl)phenylamino]- | HCID 113349 | — |
| Reactant | Potassium cyanate | HCID 11378442 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-[N-(2-cyanoethyl)anilino]ethyl N-propylcarbamate | HCID 21325795 | — |
Reaction Steps
To a mixture of 4 g. (.05 mole) of potassium cyanate and 25 ml. of sulfolane at 90° C. are added dropwise 9 ml. (12.3 g, 0.1 mole) of 1-bromopropane over a one-hour period. After 10 minutes of stirring at the same temperature, a solution of 6 g. (0.027 mole) of N-(2-cyanoethyl)-N-(2-hydroxyethyl)aniline in 5 ml. sulfolane is added. The resulting mixture is stirred at 90°-100° C. for three hours and then allowed to cool to 50° C. The mixture is poured into 1 liter of water under agitation, and the resulting layers separated. TLC of the organic layer in 4:1 benzene: acetone shows the absence of starting alcohol with the product of the above formula.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04147716 |
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| Source dataset | uspto-grants-1979_04 |
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| ORD ID | ord-31cafcba60664a8b99c5337a02869b22 |
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| Source note | uspto-grants-1979_04 |
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