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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349331Generated: October 28, 2026

Trifluoroacetic acid → (R)-6-(1-ethoxyethoxymethyl)-piperidin-2-one

https://huagongshe.com/reaction/349331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantEthyl vinyl etherHCID 8023—
ReactantSodium BicarbonateHCID 516892—
Reactant(6R)-6-(hydroxymethyl)piperidin-2-oneHCID 10887932—
SolventChloroformHCID 6212—
Product(R)-6-(1-ethoxyethoxymethyl)-piperidin-2-oneHCID 5896129380.7%

Reaction Steps

Ethyl vinyl ether (1.68 mL, 17.5 mmol) and trifluoroacetic acid (0.1 mL) were added sequentially to a solution of (R)-6-hydroxymethylpiperidin-2-one (prepared from D-α-aminoadipic acid according to Huang, et al., Synth. Commun. 1989, 19, 3485–3496, 1.62 g, 12.5 mmol) in CHCl3 (10 mL) at rt. The reaction mixture was stirred at rt for 18 h, then saturated aqueous NaHCO3 (100 mL) was added and the mixture was extracted with CH2Cl2 (3×75 mL). The combined organic phase was dried (Na2SO4), filtered and concentrated in vacuo. Purification of the residue by flash column chromatography on silica gel (CH2Cl2→4% MeOH/CH2Cl2, gradient) afforded 2.03 g (80%) of (R)-6-(1-ethoxyethoxymethyl)-piperidin-2-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179820B2
Source datasetuspto-grants-2007_02
ORD IDord-8f7a035f97e2409cbd581e2dfa942bd6
Source noteuspto-grants-2007_02