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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1484784Generated: October 31, 2026

Trifluoromethanesulfonic anhydride → 455954-80-0

https://huagongshe.com/reaction/1484784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-tert-Butyl 4-ethyl 3-oxopiperidine-1,4-dicarboxylateHCID 15852989—
SolventDichloromethaneHCID 6344—
Product455954-80-0HCID 22228415—

Reaction Steps

To a solution of 1-tert-butyl 4-ethyl 3-oxopiperidine-1,4-dicarboxylate (2.0 g, 7.37 mmol) in DCM (45 mL) was added DIPEA (1.54 ml, 8.84 mmol) and Tf2O (1.36 mL, 8.11 mmol) at −78° C., then the temperature was warmed up to room temperature and the solution was stirred at RT for 1.5 h, the mixture was diluted with DCM (100 mL), organic layer was washed with Sat. NaHCO3, brine, dried and concentrated to give 1-(tert-butyl) 4-ethyl 5-(((trifluoromethyl)sulfonyl)oxy)-3,6-dihydropyridine-1,4(2H)-dicarboxylate, which was used for next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422279B2
Source datasetuspto-grants-2016_08
ORD IDord-fbde9260dc2c44fa8c5cc9087323f7d5
Source noteuspto-grants-2016_08