HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophene → HCID 70360094, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophene | HCID 8030 | — |
| Reactant | Glycine, N-methyl-, hydrochloride (1:1) | HCID 69483 | — |
| Reactant | 2,3,4,4a,10,10a-Hexahydrophenanthren-9(1H)-one | HCID 290358 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 70360094 | HCID 70360094 | 93.8% |
Reaction Steps
A mixture of 46.4 parts of 2,3,4,4a,10,10a-hexahydro-9(1H)phenanthrenone, 58 parts of methyl glycine monohydrochloride, 2 parts of a solution of thiophene in methanol 4%, 480 parts of methanol and 26.1 parts of potassium fluoride was hydrogenated at normal pressure and at 50° C. with 3.0 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated. The residue was taken up in water and 1,1'-oxybisethane. The whole was treated with a sodium hydroxide solution. The separated organic layer was dried, filtered and evaporated, yielding 59.5 parts (93.8%) of methyl N-(1,2,3,4,4a,9,10,10a-octahydro-9-phenanthrenyl)glycine as a residue (int. 6).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04927449 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-5c1baf4c19714ba790ec4ebc584c831a |
| Source note | uspto-grants-1990_05 |