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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522277Generated: October 29, 2026

Acetic Acid → HCID 90065720, compound

https://huagongshe.com/reaction/522277

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant(1-Ethoxycyclopropoxy)trimethylsilaneHCID 2734686—
ReactantEthyl 2-(piperidin-4-yl)acetateHCID 2760465—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 90065720HCID 9006572085.1%

Reaction Steps

Sodium cyanoborohydride (2.2 g) was added to a mixture of ethyl 4-piperidine acetate (2.0 g), (1-ethoxycyclopropoxy)trimethylsilane (6.1 g), acetic acid (6.7 mL), a molecular sieve 3A (2.0 g), MeOH (20 mL), and THF (20 mL) at room temperature, and the mixture was stirred at 65° C. for 6 hours. The reaction mixture was cooled to room temperature, and concentrated under reduced pressure. After EtOAc was added to the residue, the mixture was stirred, and the insoluble material was separated by filtration. After water was added to the filtrate, potassium carbonate was added to alkalify the mixture. Extraction was performed on the mixture using EtOAc, and the extract was washed with a saturated aqueous NaHCO3 solution and saturated brine. The organic layer was dried over Na2SO4 and filtered, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (CHCl3:MeOH=100:0 to 95:5), whereby ethyl(1-cyclopropylpiperidin-4-yl)acetate (2.1 g) was obtained as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328118B2
Source datasetuspto-grants-2016_05
ORD IDord-19d8c818363041679f02ed780abfc427
Source noteuspto-grants-2016_05