HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(4-Iodophenyl)acetamide → N-(4-iodophenyl)-N-methylacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(4-Iodophenyl)acetamide | HCID 12147 | — |
| Reactant | 4-(N-methylaminocarbonyl)aminobenzoate | HCID 6928334 | — |
| Product | N-(4-iodophenyl)-N-methylacetamide | HCID 458705 | — |
Reaction Steps
The desired compound is prepared according to the method of Example 3, step2, except substituting, 4-(N-acetylamino)iodobenzene, prepared as in step 1, for 4-(N-methylaminocarbonyl)aminobenzoate
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05446062 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-07f8ce56e3f54e19bdb6128f707cc0b4 |
| Source note | uspto-grants-1995_08 |