HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Ethyl S-benzyl-(R)-cysteinate hydrochloride (1:1)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | N-tert-Butoxycarbonyl-S-benzyl-L-cysteine | HCID 2724757 | — |
| Product | Ethyl S-benzyl-(R)-cysteinate hydrochloride (1:1) | HCID 12839759 | — |
Reaction Steps
HCl(g) is bubbled into a solution of BOC-S-benzyl-L-cysteine (9.33 g, 30 mmol) in ethanol (200 mL) for 15 minutes. The container is stoppered and stirred at room temperature overnight. The solvent is evaporated in vacuo and the residue stirred in diethyl ether (150 mL) for 1.5 hours to yield S-benzyl-L-cysteine ethyl ester hydrochloride as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06992105B2 |
| Source dataset | uspto-grants-2006_01 |
| ORD ID | ord-dde0fb0d57a64215b44f51181ac6be29 |
| Source note | uspto-grants-2006_01 |