HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → HCID 53659758, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium Cyanate | HCID 517096 | — |
| Reactant | Methyl [1-(3-propylphenyl)hydrazino]acetate | HCID 54249329 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 53659758 | HCID 53659758 | 46% |
Reaction Steps
The hydrazine (Intermediate 33; 910 mg, 4.1 mmol) was dissolved in dry toluene (30 ml) under nitrogen at room temperature. Sodium cyanate (880 mg, 13.5 mmol) was added to the reaction mixture, followed by trifluoroacetic acid (0.95 ml, 12.3 mmol). The reaction was stirred at room temperature for 3 h, then poured into sodium bicarbonate solution (30 ml, 8%) and extracted with ethyl acetate (3×75 ml). The combined dried (Na2SO4), organic phases were concentrated in vacuo to give a yellow oil. The crude material was triturated with ether and hexane to give the title compound (Intermediate 34; 500 mg, 46%) as a white powdery solid m.p. 111°-116°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05023255 |
| Source dataset | uspto-grants-1991_06 |
| ORD ID | ord-eb34a55aaf6c459388c467e538309f1e |
| Source note | uspto-grants-1991_06 |