HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259605Generated: October 27, 2026
3-Aminobutanamide → 1-[p-(2-Methoxycarbonylaminovinyl)-phenoxy]-2-hydroxy-3-(2-carbamoyl-1-methyl-ethylamino)-propane
https://huagongshe.com/reaction/259605
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Aminobutanamide | HCID 10931381 | — |
| Reactant | 1-[p-(2-Methoxycarbonylaminovinyl)-phenoxy]-2,3-epoxypropane | HCID 54361820 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-[p-(2-Methoxycarbonylaminovinyl)-phenoxy]-2-hydroxy-3-(2-carbamoyl-1-methyl-ethylamino)-propane | HCID 54404419 | — |
Reaction Steps
7.5 g (0.03 mol) of 1-[p-(2-methoxycarbonylaminovinyl)-phenoxy]-2,3-epoxypropane are dissolved in 75 ml of acetonitrile and added dropwise to a boiling stirred solution of 3.34 g (0.029 mol) of β-aminobutyric acid amide in 75 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 350 ml of 0.1 N hydrochloric acid and 300 ml of ethyl acetate. The hydrochloric acid extract is separated off, rendered alkaline with sodium carbonate and extracted four times with 100 ml of ethyl acetate at a time. The organic phases are dried over sodium sulphate and evaporated under reduced pressure. The resulting oil yields 1-[p-(2-methoxycarbonylaminovinyl)-phenoxy]-2-hydroxy-3-(2-carbamoyl-1-methyl-ethylamino)-propane, of melting point 109°-111° C., from acetone-ethyl acetate.
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-d52a38ae1a4a44f182182569b9798a20 |
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| Source note | uspto-grants-1977_07 |
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