HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3alpha-Mercaptoandrostane-6,17-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Propanethiol, sodium salt (1:1) | HCID 4681725 | — |
| Reactant | 3alpha-Acetylthioandrostane-6,17-dione | HCID 86635596 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3alpha-Mercaptoandrostane-6,17-dione | HCID 86635600 | 100% |
Reaction Steps
To a suspension of 3α-acetylthioandrostane-6,17-dione (1.07 g) in MeOH (30 mL), sodium propanethiolate (0.28 g) was added and the reaction stirred for 20 minutes at room temperature. The mixture was neutralized with 1N HCl. Water was added and the mixture extracted with EtOAc. The organic layer was separated, washed with brine, and dried over Na2SO4 and evaporated to dryness to give 3α-mercaptoandrostane-6,17-dione (943 mg, 100%), used without further purification. 1H-NMR (300 MHz, DMSO-d6, ppm from TMS): δ 3.54 (1H, m), 2.77 (1H, m), 2.54 (1H, d), 2.45-1.10 (19H, m), 0.78 (3H, s), 0.66 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08536160B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-8c6096ebfeaa428da189992164337d37 |
| Source note | uspto-grants-2013_09 |