HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → N-(2-Iodophenyl)-N'-methylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1-Iodo-2-isocyanatobenzene | HCID 2733385 | — |
| Product | N-(2-Iodophenyl)-N'-methylurea | HCID 47027879 | — |
Reaction Steps
A solution of methylamine in THF (2 M, 19 mL, 39 mmol) was cooled to 0° C. and 2-iodophenylisocyanate (0.68 g, 12.6 mmol) was added dropwise over 5 minutes. The solution was stirred for 30 minutes, after which it was evaporated to dryness in vacuo to yield a white solid (2.05 g) 1H NMR (400 MHz, d6-DMSO): δ 7.81-7.77 (2H, m), 7.53 (1H, s), 7.30-7.26 (1H, m), 6.87 (1H, d, J=4.3 Hz), 6.77-6.73 (1H, m), 2.65 (3H, d, J=4.6 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07592456B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-c57c7e981afa44a383f954763034f31e |
| Source note | uspto-grants-2009_09 |