HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitrogen → HCID 54273405, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Methyl Ethyl Ketone | HCID 6569 | — |
| Reactant | Aluminum isopropoxide | HCID 11143 | — |
| Reactant | HCID 54073812 | HCID 54073812 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 54273405 | HCID 54273405 | 89.2% |
Reaction Steps
A mixture of methyl 7-hydroxy-7-methylchol-5-en-24-oate (8) (2.0 g, 4.78 mmoles), aluminum isopropoxide (1.17 g, 5.72 mmoles), 2-butanone (8.6 ml, 96 mmoles) in toluene (40 ml) was heated at 80° in a N2 atmosphere for 6 hrs. About 15 ml of solvent was distilled from the reaction mixture at atmospheric pressure. Toluene (30 ml) was added, and the mixture was extracted with 3N HCl (2 times), H2O (3 times) and dried with MgSO4. Evaporation in vacuo gave 1.7 g of an orange oil that was purified by flash chromatography on silica gel with hexane-EtOAc (7:2 and 2:1 ) to give 0.62 g of pure 9 as a colorless syrup. NMR (CDCl3): δ0.76 (s, 3H, 18-Me); 0.94 (d, 3H, 20-Me); 1.08 (s, 3H, 19-Me); 3.67 (s, 3H, CO2Me); 5.59 (s, 1H, 4H); 5.95 (s, 1H, 6-H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05595996 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-c101f9570f224e8d832caa6bf2ffc193 |
| Source note | uspto-grants-1997_01 |