HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(Chloromethyl)-2-methyl-1,1'-biphenyl → HCID 12256238, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(Chloromethyl)-2-methyl-1,1'-biphenyl | HCID 13282519 | — |
| Reactant | ([1,1'-Biphenyl]-2-yl)-N,N,N-trimethylmethanaminium iodide | HCID 13374112 | — |
| Product | HCID 12256238 | HCID 12256238 | — |
Reaction Steps
An additional method for preparing the intermediate 3-chloromethyl-2-methyl[1,1'-biphenyl] involves a Sommelet-Hauser rearrangement of N,N,N-trimethyl[1,1'-biphenyl]-2-methanaminium iodide to give 3-dimethylaminomethyl-2-methyl-[1,1'-biphenyl], which is then converted into the 3-chloromethyl derivative by treatment with ethyl chloroformate. The N,N,N-trimethyl-[1,1'-biphenyl]-2-methanaminium iodide starting material may be prepared in four steps from 2-biphenylcarboxylic acid via the acid chloride, dimethyl carboxamide, and dimethylaminomethyl derivatives.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04434182 |
| Source dataset | uspto-grants-1984_02 |
| ORD ID | ord-040befc0c99c43a1a892261cec01a560 |
| Source note | uspto-grants-1984_02 |