HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 131719172, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 18986141 | HCID 18986141 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 131719172 | HCID 131719172 | — |
Reaction Steps
Iodomethane (5 ml) was added to a stirred suspension of the product of step (b) (550 mg) in acetone (50 ml). The reaction mixture was stirred at ambient temperature for 2 days and then filtered. The collected solid was washed with acetone and dried to give methyl 4-[4-(4-methylthiocarbonimidoylphenyl)allophanoyl]phenoxyacetate, hydroiodide salt (550 mg), as a yellow solid; m.p. 216°-219° C. (decomposes); NMR Spectrum (DMSO-d6) 2.82 (3H, s), 3.71 (3H, s), 4.93 (2H, s), 7.09 (2H, d), 7.91 (4H, m), 8.05 (2H, d), 11.08 (1H, s), 11.28 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05463011 |
| Source dataset | uspto-grants-1995_10 |
| ORD ID | ord-4f9800333813450ca2bfbf58ebf02661 |
| Source note | uspto-grants-1995_10 |