HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloroethyl isocyanate → N'-(2-Chloroethyl)-N-(2,3-dihydro-1H-inden-5-yl)carbamimidic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloroethyl isocyanate | HCID 16035 | — |
| Reactant | Indan-5-amine | HCID 90496 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N'-(2-Chloroethyl)-N-(2,3-dihydro-1H-inden-5-yl)carbamimidic acid | HCID 294116 | 40% |
Reaction Steps
To a solution of 2 g of 5-aminoindane in 125 mL of anhydrous ethyl ether was 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 155°-157° C., IR (KBr pellet): 3300 (NH), 1730 (C=O, ester), and 1640 cm-1 (C=O, ureido); 1H NMR (DMSO-d6 : CDCl3): 6.96 ppm, 3.52 ppm, 3.49 ppm, 3.46 ppm, 3.43 ppm, 2.74 ppm, 2.72 ppm, 1.93 ppm. In this spectrum hydrogen present on NH groups have exchanged with the presence of DMSO-d6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05530026 |
| Source dataset | uspto-grants-1996_06 |
| ORD ID | ord-8fb45e044d094d8ebda5afeb562fcc6b |
| Source note | uspto-grants-1996_06 |