Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395366Generated: October 29, 2026

Trifluoroacetic acid → HCID 15888101, compound

https://huagongshe.com/reaction/2395366

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTrimethylsilyl isocyanateHCID 70696—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 18665573HCID 18665573—
SolventDichloromethaneHCID 6344—
ProductHCID 15888101HCID 1588810173.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05814648
Source datasetuspto-grants-1998_09
ORD IDord-dbd3d141277e4aa8ae0ea90a2f871235
Source noteuspto-grants-1998_09