HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703745Generated: October 25, 2026
Acetylethanolamine → N-(2-hydroxy-4-nitrophenoxyethyl)acetamide
https://huagongshe.com/reaction/703745
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetylethanolamine | HCID 8880 | — |
| Reactant | 1,3-Benzodioxole, 5-nitro- | HCID 75798 | — |
| Product | N-(2-hydroxy-4-nitrophenoxyethyl)acetamide | HCID 54574277 | — |
Reaction Steps
0.05 mol (8.35 g) of 3,4-methylenedioxynitrobenzene is introduced into 42 ml of N-acetylethanolamine. The mixture is heated to the region of 100° C., with stirring, and 0.055 mol (3.7 ml) of 15N potassium hydroxide solution is then added. After heating for one hour, 0.050 mol (3.3 ml) of 15N potassium hydroxide solution is added and the reaction medium is stirred at 100° C. for a further 3 hours and then poured onto 120 g of crushed ice. The unreacted starting material, which is insoluble in an alkaline medium, is filtered off. The filtrate is then acidified to pH=5.6 with hydrochloric acid in order to precipitate the expected product. It is filtered off, washed with water and dried in vacuo. It melts at 165° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04985042 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-7509ab5e4b554536b54de0f86dac2bf3 |
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| Source note | uspto-grants-1991_01 |
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