HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → s-Glycerylcysteine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Bromo-1,2-propanediol | HCID 20827 | — |
| Reactant | Cysteine Hydrochloride | HCID 60960 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | s-Glycerylcysteine | HCID 15060047 | — |
Reaction Steps
Triethylamine (6 g, 8.2 ml, 58 mmoles) was added to L-cysteine hydrochloride (3 g, 19 mmole) and 3-bromo-propan-1,2-diol (4.2 g, 2.36 ml, 27 mmole) in water and the homogeneous solution kept at room temperature for 3 days. The solution was reduced in vacuo at 40° C. to a white residue which was boiled with methanol (100 ml), centrifuged and the residue dissolved in water (5 ml). This aqueous solution was added to acetone (300 ml) and the precipitate isolated by centrifugation. The precipitate was purified by several precipitations from water with acetone to give S-(2,3-dihydroxypropyl)cysteine as a white amorphous powder (2.4 g, 12.3 mmol, 64.7%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08986700B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-8abb0f3045ab46498ee78a8d015f1766 |
| Source note | uspto-grants-2015_03 |