HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252388Generated: October 27, 2026
Formic Acid → (R)-2-methyl-2-(1-methyl-piperidin-3-yl)-propionic acid methyl ester
https://huagongshe.com/reaction/252388
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 | (R)-2-methyl-2-(1-methyl-piperidin-3-yl)-propionic acid methyl ester | HCID 66889160 | — |
Reaction Steps
0.992 g of 2-methyl-2-piperidin-3-yl-propionic acid methyl ester hydrochloride are dissolved in 2.2 ml of 2M NaOH. The solution is stirred for 10 minutes at room temperature. 7 ml of formic acid and 0.900 ml of 36% aqueous formaldehyde solution are added and the mixture is warmed to 60° C. for 16 hours. The solution is concentrated under reduced pressure. The residue is taken up water and the pH adjusted to 8-9 with saturated sodium carbonate solution. The mixture is extracted with ethyl acetate (3×) and tetrahydrofuran (2×)—the combined extracts are dried over sodium sulphate and concentrated. The title compound is obtained as a yellow oil from the residue by means of flash chromatography (SiO2 60F). Rf=0.23 (200:20:1 dichloromethane/methanol/25% conc. ammonia).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07868036B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-e8d1d230943744adb9e6cbf893f824e3 |
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| Source note | uspto-grants-2011_01 |
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