HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminofluorene → Urea, 1-(2-chloroethyl)-3-(fluoren-2-yl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminofluorene | HCID 1539 | — |
| Reactant | 2-Chloroethyl isocyanate | HCID 16035 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Urea, 1-(2-chloroethyl)-3-(fluoren-2-yl)- | HCID 276671 | 40% |
Reaction Steps
To a solution of 2 g of 2-aminofluorene in 125 mL of anhydrous ethyl ether is added dropwise 1.25 g of 2-chloroethyl isocyanate. This solution is stirred for 16 h at room temperature, cooled at -20° C., and filtered. A white solid separated and was recrystallized from ethanol (white flakes), yield 40%, mp 206°-208° C., IR (KBr pellet): 3300 (NH), 1730 (C=O, ester), and 1640 cm-1 (C=O, ureido); 1H NMR (DMSO-d6 : CDCl3): 8.08 ppm, 7.44 ppm, 7.35 ppm, 7.3 ppm, 7.27 ppm, 7.25 ppm, 7.16 ppm, 7.13 ppm, 7.02 ppm, 6.97 ppm, 6.96 ppm, 6.94 ppm, 6.93 ppm, 6.9 ppm, 6.87 ppm, 6.8 ppm, 3.5 ppm, 3.36 ppm, 3.33 ppm, 3.3 ppm, 3.25 ppm, 3.23 ppm, 3.2 ppm, 2.85 ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05750547 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-5d99e62c7cf94a0694438bde8337ca65 |
| Source note | uspto-grants-1998_05 |