HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 607493Generated: October 30, 2026
Potassium Carbonate → Methyl 6-((2-ethylhexyl)(phenyl)amino)hexanoate
https://huagongshe.com/reaction/607493
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | 2-Ethylhexyl bromide | HCID 86804 | — |
| Reactant | Methyl 6-(phenylamino)hexanoate | HCID 20441676 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 6-((2-ethylhexyl)(phenyl)amino)hexanoate | HCID 57857730 | 53,069.5% |
Reaction Steps
In a three-neck flask, methyl 6-(phenylamino)hexanoate (25.0 g, 0.113 mmol) and potassium carbonate (25.0 g, 0.169 mol) were added to dimethylformamide (100 ml) and stirred. The mixture was heated to 100° C., added with 3-(bromomethyl)heptane (26.2 g, 0.135 mol), and allowed to react with stirring for 12 hours. The reaction product was transferred into a separate funnel, and was then added with water and ethyl acetate, after which the organic layer was isolated therefrom, dehydrated using sodium sulfate, and then distilled under reduced pressure. Subsequently, the obtained material was separated through silica column chromatography, thus obtaining 20.0 g of a yellowish transparent liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07915428B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-60022c30d19b4cdf9a31f0afe1b3f257 |
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| Source note | uspto-grants-2011_03 |
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