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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227148Generated: October 29, 2026

Trifluoroacetic acid → HCID 178511763, compound

https://huagongshe.com/reaction/227148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 178454142HCID 178454142—
SolventDichloromethaneHCID 6344—
ProductHCID 178511763HCID 178511763—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of [(S)-1-(5-iodo-1H-benzoimidazol-2-yl)-2-phenyl-ethyl]-carbamic acid tert-butyl ester (1.0 g, 2.16 mmol) in dichloromethane (11 mL) at 0° C. under an atmosphere of nitrogen was added trifluoroacetic acid (6.0 mL, 81 mmol) and the mixture stirred at 0° C. with warming to room temperature over 2 hours. The reaction mixture was concentrated in vacuo then basified with saturated aqueous sodium hydrogen carbonate solution and extracted with ethyl acetate (2×25 mL). The organic extracts were combined, washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo to give (S)-1-(5-iodo-1H-benzoimidazol-2-yl)-2-phenyl-ethylamine which was used in the subsequent step without further purification (750 mg, 96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557221B2
Source datasetuspto-grants-2009_07
ORD IDord-ff1dff13a83d4da59f7e58c97b7fd761
Source noteuspto-grants-2009_07