HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920876Generated: October 30, 2026
Potassium Carbonate → HCID 123339094, compound
https://huagongshe.com/reaction/920876
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Epibromohydrin | HCID 18430 | — |
| Reactant | 3-(1H-Indol-3-yl)prop-2-enal | HCID 54058845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 123339094 | HCID 123339094 | — |
Reaction Steps
In a 10 mL Pyrex-glass vessel is mixed 3-(1H-indol-3-yl)acrylaldehyde (171 mg, 1 mmol), epibromohydrin (137 mg, 1 mmol), KOH (224 mg, 4 mmol) and anhydrous K2CO3 (553 mg, 4 mmol) in 1 mL DMF. This mixture is subjected to microwave irradiation at 350 W in successive 30 s periods, with 30 s periods at room temperature between each irradiation to avoid overheating the reaction. After the reaction has reached completion as monitored by TLC (5:1-hexanes:EtOAc) the reaction mixture is allowed to cool to room temperature and then is quenched by the addition of 10 mL 1M NaOH under vigorous stirring. The mixture is stirred for an additional 2 hrs, whereupon it is poured into 50 mL of ice-cold water. The precipitated solids are removed by filtration and washed 3×25 mL with water. The resulting solids are dried under vacuum and then recrystallized from ethanol to afford colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09273074B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-a2fb3429f868445db192c6f5bb1eaac6 |
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| Source note | uspto-grants-2016_03 |
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