HuagongsheHuagongshe Chemistry Print Report · For research reference only
alpha-Naphthyl isocyanate → HCID 9840976, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | alpha-Naphthyl isocyanate | HCID 66589 | — |
| Reactant | 3-Methoxynaphthalen-2-amine | HCID 235141 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 9840976 | HCID 9840976 | 90% |
Reaction Steps
To a solution of 2-amino-3-methoxynaphthalene (0.253 g, 1.50 mmol) in CH2Cl2 (3 mL) at room temp. was added a solution of 1-naphthyl isocyanate (0.247 g, 1.50 mmol) in CH2Cl2 (2 mL) and the resulting mixture was allowed to stir overnight. The resulting precipitate was separated and washed with CH2Cl2 to give the desired urea as a white powder (0.450 g, 90%): mp 235-236° C.; 1H-NMR (DMSO-d6) δ 4.04 (s, 3H), 7.28-7.32 (m, 2H), 7.38 (s, 1H), 7.44-7.72 (m, 6H), 7.90-7.93 (m, 1H), 8.05-8.08 (m, 1H), 8.21-8.24 (m, 1H), 8.64 (s, 1H), 9.03 (s, 1H), 9.44 (s, 1H); FAB-MS m/z 343 ((M+H)+). B1f. General Method for the Reaction of an Aryl Amine with an Aryl Isocyanate
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07517880B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-3a82f2efaa4042e68cbafd3fe773dc62 |
| Source note | uspto-grants-2009_04 |