HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227148Generated: October 29, 2026
Trifluoroacetic acid → HCID 178511763, compound
https://huagongshe.com/reaction/227148
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 178454142 | HCID 178454142 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178511763 | HCID 178511763 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07557221B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-ff1dff13a83d4da59f7e58c97b7fd761 |
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| Source note | uspto-grants-2009_07 |
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