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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2168195Generated: November 1, 2026

Water → tert-Butyl 3-methoxy-4-oxopiperidine-1-carboxylate

https://huagongshe.com/reaction/2168195

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantDi-tert-butyl dicarbonateHCID 90495—
Reactant1-Boc-3,4,4-trimethoxypiperidineHCID 59263089—
Solvent1,4-Dioxane hydrochlorideHCID 20443148—
Producttert-Butyl 3-methoxy-4-oxopiperidine-1-carboxylateHCID 57363786—

Reaction Steps

To a solution of 1,1-dimethylethyl 3,4,4-tris(methyloxy)-1-piperidinecarboxylate D17 (4.85 g) in HCl/1,4-Dioxane (50 mL) was heated at 50° C. and stirred overnight. Water (50 ml) was added to the reaction mixture and the pH adjusted to 10.0 using sodium hydroxide. After that BOC anhydride (4.22 g, 19.4 mmol) was added to the reaction mixture and stirred for 4 hours. The resulting mixture was extracted with EtOAc (3×100 ml). The organic layer was dried over anhydrous MgSO4, concentrated in vacuo to afford the desired product D18 in 3.1 g. LCMS [M-55][email protected] min (5 min run)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045485B2
Source datasetuspto-grants-2015_06
ORD IDord-545840e34cca4f5fb63f3a87db2506a7
Source noteuspto-grants-2015_06