HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643569Generated: October 30, 2026
Hydrochloric Acid → 2-methyl-3-(N-Boc-piperidine-4-yl)-propionic acid methyl ester
https://huagongshe.com/reaction/643569
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Methyl N-Boc-4-piperidinepropionate | HCID 1502093 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-methyl-3-(N-Boc-piperidine-4-yl)-propionic acid methyl ester | HCID 59261070 | — |
Reaction Steps
To a precooled (−78° C.) solution of 1.0M sodium bis(trimethylsilyl)amide in THF (13.1 mL, 13.1 mmol) was added dropwise under a nitrogen atmosphere a solution of tert-butyl 4-(3-methoxy-3-oxopropyl)piperidine-1-carboxylate (1.78 g, 6.56 mmol) in 11 mL of THF. After stirring for an additional 25 min, neat iodomethane (1.23 mL, 19.7 mmol) was added dropwise and the reaction mixture was stirred at −78° C. for two more h. The reaction mixture was then poured into 1N HCl solution and the resulting mixture was extracted twice with ether. The combined ethereal layers were washed with brine, dried over anhydrous MgSO4, filtered, and concentrated. Purification by MPLC (silica, 40% ethyl acetate/hexanes) gave tert-butyl 4-(3-methoxy-2-methyl-3-oxopropyl)piperidine-1-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700591B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-bb4dd307f2fb44cea03e5c76a819ab79 |
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| Source note | uspto-grants-2010_04 |
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