HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → S-pivaloyl-N-(S-pivaloyl-2-mercapto-2-methylpropanoyl)-L-cysteine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pivaloyl chloride | HCID 62493 | — |
| Reactant | Bucillamine | HCID 656604 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | S-pivaloyl-N-(S-pivaloyl-2-mercapto-2-methylpropanoyl)-L-cysteine | HCID 12876160 | 16.4% |
Reaction Steps
N-(2-Mercapto-2-methylpropanoyl)-L-cysteine (11.2 g, 0.05 mol) is dissolved in N sodium hydroxide (50 ml) and pivaloyl chloride (17.0 g, 0.13 mol) and aqueous N sodium hydroxide (150 ml) are added dropwise at 0° C. with stirring under a nitrogen atmosphere. After the addition, the mixture is stirred for 1 hour at room temperature and acidified with 6 N hydrochloric acid. The produced oil is extracted with ethyl acetate and the organic layer is washed with water, dried and concentrated to dryness under reduced pressure to yield 3.2 g (16.4%) of S-pivaloyl-N-(S-pivaloyl-2-mercapto-2-methylpropanoyl)-L-cysteine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04255446 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-7c4dd1599f7b4ac3a70bf509b882be75 |
| Source note | uspto-grants-1981_03 |