HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374440Generated: October 30, 2026
Ethanolamine → 5-Cyano-(2-hydroxyethyl)salicylamide
https://huagongshe.com/reaction/374440
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Methyl 5-cyano-2-hydroxybenzoate | HCID 10583428 | — |
| Product | 5-Cyano-(2-hydroxyethyl)salicylamide | HCID 18997111 | — |
Reaction Steps
A solution of 9.7 g (0.547 mole) of 5-cyanosalicylic acid methyl ester (prepared as described in Chem. Pharm. Bull., 1984, 38, 4466-4477) in 15 ml of acetonitrile, was combined with 4.01 g (0.65 mole) of ethanolamine, and then heated at reflux for 24 hours. At the end of the 4th and 7th hours, two further portions of 1 g (0.016 mole) each of ethanolamine were added. At the end of the heating, the solution was evaporated to dryness under vacuum, taken up with ethyl acetate and washed with hydrochloric acid 1N and then with water. The organic layer was dried over sodium sulphate and concentrated to small volume. The formed solid was filtered and dried under vacuum yielding 9.2 g of 5-cyano-(2-hydroxyethyl)salicylamide. m.p. 144°-146° C. (acetonitrile).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05480882 |
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| Source dataset | uspto-grants-1996_01 |
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| ORD ID | ord-89f42e1be6a04a159f008a6dc178f94a |
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| Source note | uspto-grants-1996_01 |
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