HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dehydroepiandrosterone → 1476-64-8
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dehydroepiandrosterone | HCID 5881 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Ethyl cysteinate hydrochloride | HCID 2723617 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1476-64-8 | HCID 7056608 | — |
Reaction Steps
Following the procedure described by Djerassi (C. Djerassi, N. Crossley and M. A. Kielczewski, J. Org. Chem. 27, 1112, 1962), dehydroepiandrosterone (2.88 g, 10 mmol) is dissolved in anhydrous ethanol, sodium acetate is added followed by L-cysteine ethyl ester hydrochloride (18 g, 100 mmol) and the mixture is heated overnight under an argon atmosphere. The reaction mixture is then evaported under vacuum. Methylene chloride is added to precipitate excess of L-cysteine ethyl ester hydrochloride . The solution is then filtered and the filtrate is washed twice with water, dried on magnesium sulfate, filtered and evaporated under vacuum. The residue is triturated with ethanol to give crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05837700 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-0cfcd35fefc24132be84cef66253e5d0 |
| Source note | uspto-grants-1998_11 |