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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744679Generated: October 30, 2026

Trifluoromethanesulfonic anhydride → 455954-80-0

https://huagongshe.com/reaction/1744679

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 2222841565.1%

Reaction Steps

Trifluoromethanesulfonic anhydride (12.4 mL, 73.7 mmol) was added over approximately 0.1 h, via syringe, to a stirred solution of the product of step B (27.1 g, 67.0 mmol) and N,N-diisopropylethylamine (14.0 mL, 80.4 mmol) in methylene chloride (250 mL) at −78° C. After allowing to warm to ambient temperature overnight, the reaction mixture was quenched with saturated aqueous sodium bicarbonate, poured into water and extracted three times with methylene chloride. The combined organic extracts were washed with brine, dried (MgSO4) and concentrated in vacuo. Purification of the residue by flash chromatography on silica gel (gradient elution; 0–20% ethyl acetate/hexanes as eluent) afforded the title compound as an amber colored oil (17.6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07015235B2
Source datasetuspto-grants-2006_03
ORD IDord-39ec9578abbe4cd8b0bd37917c37e8f9
Source noteuspto-grants-2006_03