HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl orthoformate → HCID 22827147, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | HCID 22827146 | HCID 22827146 | — |
| Reactant | HCID 22827148 | HCID 22827148 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22827147 | HCID 22827147 | — |
Reaction Steps
Following the procedure of Example 3, substituting trans-(±)-3,4-difluoro-N-methyl-N-[6-oxo-2-(1-azetidinyl)cyclohexyl]benzeneacetamide for the trans-(±)-3,4-dichloro-N-methyl-N-[6-oxo-2-(1-pyrrolidinyl)cyclohexyl]benzeneacetamide in 50 ml of dry ethanol instead of methanol and 5.0 ml of triethylorthoformate instead of trimethylorthoformate, there is formed as product trans-(±)-3,4-difluoro-N-methyl-N-[6,6-diethoxy-2-(1-azetidinyl)cyclohexyl]benzeneacetamide, which is converted to a hydrochloride salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04460600 |
| Source dataset | uspto-grants-1984_07 |
| ORD ID | ord-90c93ab025004fe6a95a1575b1591915 |
| Source note | uspto-grants-1984_07 |