HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1446880Generated: October 25, 2026
Potassium Carbonate → HCID 13314825, compound
https://huagongshe.com/reaction/1446880
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 2-bromopropionate | HCID 79040 | — |
| Reactant | 4-[N-Methyl-N-(6-bromo-2-benzoxazolyl)amino]phenol | HCID 13314820 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | HCID 13314825 | HCID 13314825 | 53.7% |
Reaction Steps
A mixture of 4-[N-methyl-N-(6-bromo-2-benzoxazolyl)amino]phenol (0.6, 0.002 mole), ethyl 2-bromopropionate (0.4 g, 0.002 mole), anhydrous potassium carbonate (0.3 g, 0.002 mole) and methyl ethyl ketone (6 ml) was heated under reflux, with stirring, for a period of 3 hours. Thin layer chromatography indicated that the reaction had not gone to completion and therefore further anhydrous potassium carbonate (0.15 g) and methyl ethyl ketone was added and the mixture was heated under reflux for a further period of 3 hours. The solvent was removed by distillation under reduced pressure, water (50 ml) was added to the residue and the aqueous mixture was extracted with diethyl ether (3×30 ml). The combined extracts were washed with brine, dried over anhydrous magnesium sulfate and the solvent was evaporated to give a dark red oil. The oil was heated at a temperature of 100° C. at a pressure of 0.1 mm Hg for a period of 2 hours to remove residual ethyl 2-bromopropionate and the residue was recrystallised from hexane/cyclohexane to give the title compound as a white solid (0.45 g), mp 91°-92° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04314065 |
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| Source dataset | uspto-grants-1982_02 |
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| ORD ID | ord-bf9ccb253a364288b7ba29f9a3654b5e |
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| Source note | uspto-grants-1982_02 |
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