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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522414Generated: October 31, 2026

2,2,2-Trifluoroethyl trifluoromethanesulfonate → HCID 117598746, compound

https://huagongshe.com/reaction/522414

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,2-Trifluoroethyl trifluoromethanesulfonateHCID 80366—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 117598881HCID 117598881—
SolventAcetonitrileHCID 6342—
ProductHCID 117598746HCID 117598746—

Reaction Conditions

Temperature55 °C

Reaction Steps

To a solution of the product from Step 1 (101 mg, 0.102 mmol) in acetonitrile (5 mL) was added Hunig's base (0.089 mL, 0.511 mmol) followed by 2,2,2-trifluoroethyl trifluoromethanesulfonate (71.1 mg, 0.306 mmol). The reaction was stirred at 55° C. for 3 hours after which it was quenched with water and extracted with EtOAc. Purification by PTLC (3% MeOH in CH2Cl2) followed by reverse phase HPLC (0 to 90% acetonitrile in water; with 0.1% HCOOH) provided the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328138B2
Source datasetuspto-grants-2016_05
ORD IDord-842ed8e2b6ee423bbe89887b2c74b90e
Source noteuspto-grants-2016_05