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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1869476Generated: October 26, 2026

Glycolic Acid → 4-(5-Hydroxymethyl-[1,2,4]oxadiazol-3-yl)-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1869476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycolic AcidHCID 757—
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
ReactantIsobutyl chloroformateHCID 62365—
ReactantHCID 178451986HCID 178451986—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product4-(5-Hydroxymethyl-[1,2,4]oxadiazol-3-yl)-piperidine-1-carboxylic acid tert-butyl esterHCID 57986906—

Reaction Steps

To a solution of hydroxy-acetic acid (1.67 g, 22 mmol), NEt3 (4.4 g, 44 mmol) in toluene (150 mL) was added isobutylchloroformate (6 g, 44 mmol) at 0° C. The mixture was stirred at room temperature for 1.5 hours. 4-(N-Hydroxycarbamimidoyl)-piperidine-1-carboxylic acid tert-butyl ester (5.35 g, 22 mmol) was added to the mixture. The mixture was heated under reflux overnight, and then cooled to room temperature; the mixture was washed successively with H2O and brine. After drying (Na2SO4), the solvent was removed. The residue was dissolved in THF (20 mL), and aqueous NaOH (10 mL, 10 mmol) was added. The mixture was stirred at room temperature for 2 hours and diluted with EtOAc (50 mL). The organic layer was washed with brine, after drying (Na2SO4), the solvent was removed in vacuo, and the residue was purified by silica column chromatography with EtOAc/hexanes to afford the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07638541B2
Source datasetuspto-grants-2009_12
ORD IDord-44427f527de3447f8e2131c9154fcaf7
Source noteuspto-grants-2009_12