HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395366Generated: October 29, 2026
Trifluoroacetic acid → HCID 15888101, compound
https://huagongshe.com/reaction/2395366
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Trimethylsilyl isocyanate | HCID 70696 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 18665573 | HCID 18665573 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15888101 | HCID 15888101 | 73.1% |
Reaction Steps
To a solution of N,O-di(tert-butoxycarbonyl)-[3-[3-(4,5-dihydro-4(R)-phenyl-oxazol-2-yl)phenyl]-2-propyn-1-yl]hydroxylamine (1.99 g, 4 mmol) in dichloromethane (30 ml) cooled to 0° C. was slowly added trifluoroacetic acid (10 ml). The reaction mixture was allowed to warm to room temperature, stirred an additional 30 min., and then poured into a saturated aqueous NaHCO3 solution (100 ml). The mixture was extracted with dichloromethane (3×30 ml) and the organic phase washed with brine (20 ml), dried (MgSO4) and evaporated. The resulting residue was dissolved in tetrahydrofuran (20 ml) and trimethylsilyl isocyanate (0.84 ml, 6.3 mmol) added. After stirring for 10 min. precipitation of product occurred. Methanol (1 ml) was added and solvent was removed by evaporation. The resulting solids were recrystallized from ethyl acetate to afford the title compound (0.98 g, 72 %) as white solids.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05814648 |
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| Source dataset | uspto-grants-1998_09 |
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| ORD ID | ord-dbd3d141277e4aa8ae0ea90a2f871235 |
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| Source note | uspto-grants-1998_09 |
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