HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423214Generated: October 30, 2026
Boric Acid → 2-Ethoxy-4-(3-((S)-3-methy-1-(2-piperidin-1-yl-phenyl)-butylamino)-2-oxo-propyl)-benzoic acid ethyl ester
https://huagongshe.com/reaction/423214
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boric Acid | HCID 7628 | — |
| Reactant | 3-Ethoxy-4-ethoxycarbonylphenylacetic acid | HCID 10131212 | — |
| Reactant | 3-Methyl-1-(2-piperidinophenyl)-1-butylamine, (S)- | HCID 10514609 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Ethoxy-4-(3-((S)-3-methy-1-(2-piperidin-1-yl-phenyl)-butylamino)-2-oxo-propyl)-benzoic acid ethyl ester | HCID 10648419 | 73.3% |
Reaction Steps
In a round bottom flask fitted with a dean stark condenser, (S)-3-methyl-1-(2-piperidinophenyl)-1-butylamine (10 g, 0.0406 mol) was dissolved in toluene (100 ml), followed by the addition of 3-ethoxy-4-ethoxycarbonyl phenyl acetic acid (10.26 g, 0.0407 mol) and boric acid (0.26 g, 0.0042 mol). The reaction mixture was refluxed for 16-18 hours. The resulting mass was then cooled to 25-30° C. followed by filtration. The filtrate was washed with water and 1.0% sodium bicarbonate solution followed by complete distillation of toluene and the resulting residue was stirred with hexane (50 ml) for 1 hour. The precipitated solid was filtered and washed with hexane (10 ml). The wet product was dried at 50-55° C. under vacuum for 4-6 hours to produce Ethyl (S)-2-ethoxy-4-[N-(1-(2-piperidino-phenyl)-3-methyl-1-butyl)-aminocarbonyl methyl]-benzoate (Yield=73.3%; HPLC Purity: 99.50%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08101769B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-22778ac9720749c5aa3d48fdb7d40014 |
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| Source note | uspto-grants-2012_01 |
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