HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → HCID 19775943, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 2-Aminopropanol | HCID 5126 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 19775929 | HCID 19775929 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 19775943 | HCID 19775943 | 95.1% |
Reaction Steps
The dinitrobenzene obtained in Step A (10.0 g, 24.3 mmol) was dissolved in N,N-dimethylformamide (60 cm 3). Triethylamine (5.1 cm3, 36.5 mmol) and DL 2-aminopropanol 2.9 cm3, 36.5 mmol) were added, and the mixture was stirred at room temperature for 21 hours, and then heated at 70° C. for a further 3 hours. The mixture was cooled to room temperature, poured into diethyl ether (500 cm3) and washed with water (3×300 cm3). The organic layer was dried (MgSO4), filtered and evaporated under reduced pressure to give DL 2-[5-(4-bromo-1-methyl-5-trifluoromethyl-1H-pyrazol -3-yloxy)-2-nitrophenylamino]propan-1-ol (10.15 g) as an orange solid m.p 116°-118° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05190574 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-fcd9252c8177417794a546e36dcbcb52 |
| Source note | uspto-grants-1993_03 |