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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173842Generated: November 2, 2026

Trifluoroacetic acid → HCID 67983601, compound

https://huagongshe.com/reaction/2173842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 68062013HCID 68062013—
SolventDichloromethaneHCID 6344—
ProductHCID 67983601HCID 67983601—

Reaction Steps

Part A: A round bottom flask was charged with (±)-ethyl 4-(1-((tert-butoxycarbonyl)(5-(4-(trifluoromethyl)phenyl)pyrazin-2-yl)amino)butyl)benzoate (4.85 g, 8.92 mmol), DCM (60 mL) and TFA (15 mL). Reaction mixture stirred at room temperature for 3 hours. Sodium bicarbonate (sat. aq.) used to quench the excess TFA and the aqueous layer is extracted with DCM (3×). Combined organics washed with water (1×), brine (1×), dried over sodium sulfate filtered and concentrated to provide (±)-ethyl 4-(1-((5-(4-(trifluoromethyl)phenyl)pyrazin-2-yl)amino)butyl)benzoate as a crude orange gum (4.01 g, quant.). No further purification before next step. MS (M+1): 444.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056834B2
Source datasetuspto-grants-2015_06
ORD IDord-18e0a07ad0224183a400d330ee0d6b3d
Source noteuspto-grants-2015_06