HuagongsheHuagongshe Chemistry Print Report · For research reference only
16alpha-Hydroxyestrone → HCID 22837741, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 16alpha-Hydroxyestrone | HCID 115116 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Butyric anhydride | HCID 7798 | — |
| Product | HCID 22837741 | HCID 22837741 | 80.6% |
Reaction Steps
A solution of 2.0 g of 3,16α-dihydroxy-1,3,5(10)-estratrien-17-one in 10 ml of pyridine and 5 ml of butyric anhydride is allowed to stand at room temperature for 15 hours with the addition of 100 mg of 4-dimethylaminopyridine. The reaction mixture is diluted with diethyl ether, washed with water, dried over sodium sulfate, and evaporated. The residue is chromatographed on silica gel with a pentane-diethyl ether gradient (0-30% diethyl ether), yielding 1.2 g of 3,16α-dibutyryloxy-1,3,5(10)-estratrien-17-one as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04738957 |
| Source dataset | uspto-grants-1988_04 |
| ORD ID | ord-027f42199d994f3da6a10723bc7f7c52 |
| Source note | uspto-grants-1988_04 |