HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → HCID 66641138, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | HCID 43313256 | HCID 43313256 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 66641138 | HCID 66641138 | — |
Reaction Steps
In a manner similar to the method described in Example 112b, 2-(4-cyano-phenyloxy)-5-fluoro-benzaldehyde was treated with LHMDS, acetyl chloride, triethylamine and chloro-trimethyl-silane to give the desired compound, which was directly used for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08134001B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-701b87f7b6204a36a050a3e30b870dba |
| Source note | uspto-grants-2012_03 |