HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → HCID 67364108, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | HCID 67361589 | HCID 67361589 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 67364108 | HCID 67364108 | 56% |
Reaction Steps
Triethyl orthoformate (3 ml, 18 mmol) and p-Toluenesulfonic acid (30 mg, 0.16 mmol) were added to a suspension of 15α-acetoxy-18-methyl-estr-4-en-3,17-dione (3 g, 8.8 mmol) in EtOH (18 ml). The mixture was stirred at room temperature for 1 h. Ammonia 32% (15.4 ml, 145 mmol) was added, and the mixture was heated at 40° C. for 48 h, cooled to 10° C., and ethyl acetate and water (15 ml) were then added. The extract was washed with water and concentrated. The crude product was purified by flash chromatography, eluting with heptane and ethyl acetate (8:2), crystallized from heptane, and dried under vacuum to afford 3-ethoxy-18-methyl-estra-3,5,15-trien-17-one (1.54 g, yield: 56%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09012667B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-edd664a4d3b5404cb0c94275c0b0239d |
| Source note | uspto-grants-2015_04 |