HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → S-Acetylglutathione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Pivaloyl chloride | HCID 62493 | — |
| Reactant | Glutathione | HCID 124886 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Propan-2-one--water (1/1) | HCID 18366337 | — |
| Product | S-Acetylglutathione | HCID 9894372 | 85% |
Reaction Steps
Using in the procedure of Example 1 acetyl chloride, in place of pivaloyl chloride, L-glutathione reduced (15.4 g) provides, after usual work-up, a crude white solid which is dissolved in warm acetone/water (2/1; 40° C.; 300 ml). The obtained solution is further diluted with more acetone (100 ml) and cooled on ice-water bath. After about two hours the white crystalline precipitate is collected, washed with the solvent (40 ml) and dried under vacuum affording γ-L-glutamyl-S-acetyl-L-cysteinyl-glycine (14.8 g yield=85%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05382679 |
| Source dataset | uspto-grants-1995_01 |
| ORD ID | ord-d42a66c30acc43119a0bad79addf5c0c |
| Source note | uspto-grants-1995_01 |