HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452281Generated: November 1, 2026
2-(Methylamino)ethanol → HCID 19972386, compound
https://huagongshe.com/reaction/1452281
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(Methylamino)ethanol | HCID 8016 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 13122092 | HCID 13122092 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 19972386 | HCID 19972386 | — |
Reaction Steps
A solution of 1.6 ml of 2-methylamino-ethanol in 10 ml of water was added dropwise over a period of 5 minutes to a suspension of 6 g of 3-methyl-4-oxo-2-phenyl-4H-1-benzopyran-8-carbonyl chloride and 1.52 g of potassium carbonate in 60 ml of acetone. After stirring for 2.5 hours at 20°-25° C., the solvent was removed in vacuo and the residue was taken up in 150 ml of acetone. The mixture was refluxed for 15 minutes, and was then filtered. The solvent was evaporated from the filtrate and the residue was dissolved in 20 ml of dimethylformamide, treated with 14 ml of 1.4% aqueous sodium carbonate solution, stirred for 30 minutes at 20°-25° C. and diluted by addition of 150 ml of water. The mixture was extracted with chloroform and the organic layer was washed with 0.5N aqueous hydrochloric acid solution and then with water. The solution was dried over anhydrous sodium sulfate and the chloroform was evaporated off. The resulting oil was taken up in 200 ml of diethyl ether and stirred for 2 hours at 20°-25° C. The solids were collected by filtration and crystallized from ethyl acetate to give 4.97 g of the title compound, m.p. 128°-130° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05605896 |
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| Source dataset | uspto-grants-1997_02 |
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| ORD ID | ord-64077693420844a5af9c7eab9c25ffc0 |
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| Source note | uspto-grants-1997_02 |
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