Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | HCID 1551691 | HCID 1551691 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 801657 | HCID 801657 | — |
Reaction Steps
To a solution of (R)-2-(1,3-dioxoisoindolin-2-yl)-4-(methylthio)butanoic acid (87.124 g, 312 mmol) from preparation 54 in methanol (750 ml) was added hydrogen peroxide (pre-cooled to −30° C.; 38.9 g, 343 mmol) in methanol (250 ml) at −20° C. The reaction mixture was stirred at −20° C. overnight (by use of a cryostat) then warmed to rt over a further 24 hours then to 30° C. for 5 h, LCMS suggesting 95% conversion. The reaction mixture was evaporated under vacuum to give the title compound as a mixture of diastereoisomers that were progressed directly in preparation 3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08598123B2 |
|---|
| Source dataset | uspto-grants-2013_12 |
|---|
| ORD ID | ord-35f489a6c1894ebead06274d898e2336 |
|---|
| Source note | uspto-grants-2013_12 |
|---|