HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1069088Generated: October 28, 2026
Trifluoroacetic acid → HCID 21191156, compound
https://huagongshe.com/reaction/1069088
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 54336416 | HCID 54336416 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21191156 | HCID 21191156 | 98.5% |
Reaction Steps
The methyl-3′-[2-[[(tert-butoxy)carbonyl]amino]ethoxy]-[1,1′-biphenyl]-3-carboxylate (659 mg) was dissolved in methylene chloride (25 mL) and trifluoroacetic acid (2.5 mL) was added. The mixture was stirred at room temperature for 6 h, additional trifluoroacetic acid (1.0 mL) was added and the mixture was stirred overnight. The mixture was concentrated and partitioned between saturated aqueous sodium bicarbonate and ethyl acetate. The organic layer was separated, dried over sodium sulfate, filtered and concentrated to give the crude product. This residue was partitioned between 1:1 hexane: ethyl acetate and 1 N aqueous HCl. The aqueous layer was separated, washed with 1:1 hexane: ethyl acetate and made basic by addition of solid sodium bicarbonate. The mixture was extracted twice with ethyl acetate, and the combined organic extracts were dried over sodium sulfate, filtered and concentrated to afford the title compound (474 mg) as a colorless oil. Electrospray MS (positive ion): (M+H) 272.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06251925B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-66f9ec29f64b4aac90bd651018e8bb33 |
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| Source note | uspto-grants-2001_06 |
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