HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2237749Generated: October 27, 2026
Formic Acid → 2-Methyl-2-(1-methyl-piperidin-3(r,s)-yl)-propionic acid methyl ester
https://huagongshe.com/reaction/2237749
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Methyl 2-methyl-2-(piperidin-3-yl)propanoate hydrochloride | HCID 66887928 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 2-Methyl-2-(1-methyl-piperidin-3(r,s)-yl)-propionic acid methyl ester | HCID 66889161 | — |
Reaction Steps
0.370 g of 2-methyl-2-piperidin-3(R,S)-yl-propionic acid methyl ester hydrochloride (Example 142) are dissolved in 0.5 ml of 3M NaOH. 2 ml of formic acid and 0.19 ml of formaldehyde (35% aqueous solution) are added and the reaction solution is warmed to 60° C. for 20 hours. The solution is cooled to room temperature, neutralised with 3M NaOH to pH 8-9 and extracted with dichloromethane (3×10 ml). The combined organic phases are washed with water (10 ml), dried over sodium sulphate and concentrated by evaporation. The residue is purified by means of flash chromatography (SiO2 60F) to provide the title compound as a colourless oil. Rf 0.19 (200:20:1 dichloromethane-methanol-25% conc. ammonia).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07718675B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-4486f4cfc0254e2a83dd041046e510d9 |
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| Source note | uspto-grants-2010_05 |
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