HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 4-[N-(2-Benzyloxy-5-bromophenethyl)-N-methylamino]benzoic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | ethyl 4-[N-(2-benzyloxy-5-bromophenethyl)-N-methylamino]benzoate | HCID 22675492 | — |
| Reactant | ethyl 4-[N-(2-benzyloxy-5-bromophenethyl)amino]benzoate | HCID 22675521 | — |
| Product | 4-[N-(2-Benzyloxy-5-bromophenethyl)-N-methylamino]benzoic Acid | HCID 22675493 | — |
Reaction Steps
Ethyl 4-[N-(2-benzyloxy-5-bromophenethyl)amino]benzoate was converted to ethyl 4-[N-(2-benzyloxy-5-bromophenethyl)-N-methylamino]benzoate using a similar method to that described in Example 41(D) except methyl iodide was used in place of iodoethane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06787562B2 |
| Source dataset | uspto-grants-2004_09 |
| ORD ID | ord-15f479a5e6774363abecd0ff2d70645e |
| Source note | uspto-grants-2004_09 |