HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → HCID 20303318, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | HCID 20303309 | HCID 20303309 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 20303318 | HCID 20303318 | — |
Reaction Steps
Reduction of the ethyl 2,3-dibenzyl-2-azabicyclo[2.2.2]oct-5-ene-7-carboxylic described in Example 1AE in the form of the hydrochloride salt with one molar equivalent of hydrogen over a palladium-on-charcoal catalyst at ambient temperature and reaction of the resulting ethyl 3-benzyl-2-azabicyclo[2.2.2]oct-5-ene-7-carboxylate with acetyl chloride in the presence of pyridine affords ethyl 2-acetyl-3-benzyl-2-azabicyclo[2.2.2]oct-5-ene-7-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04100164 |
| Source dataset | uspto-grants-1978_07 |
| ORD ID | ord-d856489250eb433197188c4fbda7f549 |
| Source note | uspto-grants-1978_07 |