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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257747Generated: November 3, 2026

Sodium Carbonate → Phenylmethyl 3-(aminocarbonyl)-3-methyl-1-piperidinecarboxylate

https://huagongshe.com/reaction/1257747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantBenzyl chloroformateHCID 10387—
Reactant1,4-DioxaneHCID 31275—
ReactantHCID 67323401HCID 67323401—
SolventWaterHCID 962—
ProductPhenylmethyl 3-(aminocarbonyl)-3-methyl-1-piperidinecarboxylateHCID 67324533409.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3-Methyl-piperidine-3-carboxylic acid amide hydrochloride (740 mg, 4.1 mmol) in a cosolvent of 1,4-dioxane and water (12 mL, v:v=5:1) was added sodium carbonate (1.6 g, 15 mmol). The mixture was cooled to 0° C., benzyl chloroformate (900 mg, 0.53 mmol) was added, and the mixture was allowed to stir at room temperature for 3 h. LCMS showed starting material was consumed. The volatile components were removed, and the residue was extracted with ethyl acetate, purified by column chromatography (eluting with 10% methanol in dichloromethane) to give 600 mg (53%) of 3-Carbamoyl-3-methyl-piperidine-1-carboxylic acid benzyl ester. LCMS (Method K, ESI): RT=1.18 min, m+Na=298.8; 1H NMR (400 MHz, CDCl3) δ: 7.32-7.23 (m, 5H), 5.07-5.03 (m, 2H), 4.30-4.10 (m, 1H), 4.10-3.90 (m, 1H), 3.10-2.40 (m, 2H), 1.65-1.75 (m, 2H), 1.60-1.30 (m, 2H), 1.25-1.15 (m, 1H), 1.09 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461328B2
Source datasetuspto-grants-2013_06
ORD IDord-9f8fb9ad67004763bed63166227dd773
Source noteuspto-grants-2013_06