HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729012Generated: October 30, 2026
Hydrochloric Acid → HCID 54003055, compound
https://huagongshe.com/reaction/729012
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 3-aminopropanoate | HCID 419889 | — |
| Reactant | 2-(Oxiran-2-ylmethoxy)benzonitrile | HCID 12619671 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 54003055 | HCID 54003055 | — |
Reaction Steps
15.36 g of the hydrochloride of ethyl 3-aminopropanoate and 6.2 g of potassium hydroxide were stirred in 150 ml of abs. ethanol until neutral reaction, ca 1 h. Under reflux was added 8.7 g of 2-(2,3-epoxypropoxy)benzonitrile in 125 ml of abs. ethanol. The mixture was refluxed for 8 h, filtered and evaporated. The residue was dissolved in ether, washed twice with water and extracted with 25 ml of 2-n hydrochloric acid. The aqueous phase was extracted with methylene chloride. The methylene chloride phase was dried over Na2SO4, filtered and evaporated to dryness. The hydrochloride of ethyl N-[3-(2-cyanophenoxy)-2-hydroxypropyl]-3-aminopropanoate crystallized. Yield 5.75 g. Melting point 120° C. (HCl). The structure was determined using NMR and equivalent weight.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05051446 |
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| Source dataset | uspto-grants-1991_09 |
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| ORD ID | ord-cc46c5ec84a14c2caee42c63827d47f9 |
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| Source note | uspto-grants-1991_09 |
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