HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196978Generated: November 1, 2026
Trifluoroacetic acid → HCID 19897021, compound
https://huagongshe.com/reaction/1196978
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Cyclohexyl isocyanate | HCID 18502 | — |
| Reactant | HCID 19897004 | HCID 19897004 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 19897021 | HCID 19897021 | — |
Reaction Steps
2-Amino-4'-benzyloxypropiophenone hydrochloride (349 mg, 1.20 mmol) was suspended in acetone (30 ml) under ice-cooling, and cyclohexyl isocyanate (204 mg, 1.62 mmol) was added thereto. Triethylamine (377 mg, 3.73 mmol) was then added, and the mixture was stirred for one hour under ice-cooling. After addition of trifluoroacetic acid (2 ml), the mixture was stirred for 6 days at room temperature. The solvent was removed by evaporation in vacuo, and the residue was extracted with dichloromethane. The extract was washed successively with water and saturated aqueous sodium chloride, and dried over anhydrous magnesium sulfate. Evaporation of the solvent provided a crude product, which was purified by column chromatography (chloroform/ ethanol=50/1 (v/v)) and recrystalization (ethanol-chloroform) to give the title compound. Yield: 240 mg (55%), m.p. 262° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05116858 |
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| Source dataset | uspto-grants-1992_05 |
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| ORD ID | ord-8d31af39086b4792ba8b0fb8ccc3eb7c |
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| Source note | uspto-grants-1992_05 |
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