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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972390Generated: November 1, 2026

Trifluoroacetic acid → 3-(tetrahydro-2H-pyran-4-ylmethyl)-2,5-piperazinedione

https://huagongshe.com/reaction/1972390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactantmethyl N-(tert-butoxycarbonyl)-3-(tetrahydro-2H-pyran-4-yl)-L-alanylglycinateHCID 66582350—
SolventDichloromethaneHCID 6344—
Product3-(tetrahydro-2H-pyran-4-ylmethyl)-2,5-piperazinedioneHCID 6658249877.9%

Reaction Steps

A 250 mL round-bottomed flask was charged with methyl N-(tert-butoxycarbonyl)-3-(tetrahydro-2H-pyran-4-yl)-alanylglycinate (3.00 g, 8.71 mmol), 10 mL of CH2Cl2, and 5 mL of TFA. After 10 min, the mixture was concentrated then re-dissolved in MeOH (50 mL) and triethylamine (10 mL) and then heated at reflux for 18 h. After that time, the white precipitate formed was collected by filtration to give 3-(tetrahydro-2H-pyran-4-ylmethyl)-2,5-piperazinedione (1.44 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431563B2
Source datasetuspto-grants-2013_04
ORD IDord-07cb484798a040cfaf1d5c6083298acb
Source noteuspto-grants-2013_04