HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259606Generated: October 27, 2026
Butyronitrile, 3-amino- → HCID 53921112, compound
https://huagongshe.com/reaction/259606
Participants
| Role | Name | HCID | Charge |
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| Reactant | Butyronitrile, 3-amino- | HCID 123366 | — |
| Reactant | 1-[p-(2-Methoxycarbonylaminovinyl)-phenoxy]-2,3-epoxypropane | HCID 54361820 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 53921112 | HCID 53921112 | — |
Reaction Steps
3.0 g (0.012 mol) of 1-[p-(2-methoxycarbonylaminovinyl)-phenoxy]-2,3-epoxypropane are dissolved in 25 ml of acetonitrile and added dropwise to a boiling stirred solution of 0.96 g (0.011 mol) of β-aminobutyronitrile in 20 ml of acetonitrile. The mixture is stirred for 20 hours under reflux, the solvent is removed by distillation under reduced pressure and the oil which remains is partitioned between 150 ml of 0.1 N hydrochloric acid and 100 ml of ethyl acetate. The hydrochloric acid extract is separated off, rendered alkaline with sodium carbonate and extracted four times with 50 ml of ethyl acetate at a time. The organic phases are dried over sodium sulphate and evaporated under reduced pressure. The resulting oil solidifies on cooling to give crystals of 1-[p-(2-methoxycarbonylaminovinyl)-phenoxy]-2-hydroxy-3-(2-cyano-1-methylethyl-amino)-propane of melting point 122°-123° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04038414 |
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| Source dataset | uspto-grants-1977_07 |
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| ORD ID | ord-b1902f097d6745db88b517ac4df082f3 |
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| Source note | uspto-grants-1977_07 |
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