HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Ethyl L-cysteinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl cysteinate hydrochloride | HCID 2723617 | — |
| Catalyst | HCID 178418647 | HCID 178418647 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl L-cysteinate | HCID 13359 | 293.9% |
Reaction Steps
1.3 g of sulfodehydroabietic acid is dissolved in 15 ml of ethanol and 0.472 mg of silver carbonate and 20 ml of water are added thereto. 0.635 g of ethyl L-cysteinate hydrochloride are added to the mixture and said mixture is stirred at room temperature. The precipitates are filtered off and the filtrate is concentrated to dryness under reduced pressure. The residue is recrystallized from a mixture of methanol and ethyl acetate, whereby 1.5 g of sulfodehydroabietic acid ethyl L-cysteinate salt hemihydrate is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04529602 |
| Source dataset | uspto-grants-1985_07 |
| ORD ID | ord-44d69d7bac994cddb8d765ad2efb1853 |
| Source note | uspto-grants-1985_07 |