HuagongsheHuagongshe Chemistry Print Report · For research reference only
7,7-Dioxo-5,6-dihydrothieno[2,3-b]thiopyran-4-one → (R)-(+)-5,6-Dihydro-4H-thieno[2,3-b]-thiopyran-4-ol-7,7-dioxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7,7-Dioxo-5,6-dihydrothieno[2,3-b]thiopyran-4-one | HCID 3613959 | — |
| Reactant | (Dimethyl sulfide)trihydroboron | HCID 12423031 | — |
| Reactant | HCID 178419238 | HCID 178419238 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (R)-(+)-5,6-Dihydro-4H-thieno[2,3-b]-thiopyran-4-ol-7,7-dioxide | HCID 1480164 | — |
Reaction Conditions
| Temperature | -15 °C |
|---|
Reaction Steps
To a magnetically stirred solution of 5,6-Dihydro-4H-thieno[2,3-b]-thiopyran-4-one-7,7-dioxide (13) (1.00 g, 4.94 mmol) in dry THF (14 mL) was added (S)-diphenylprolinol-borane complex from Example 12 (132 mg, 0.494 mmol). The solution was cooled to -15° C. and a solution of borane-dimethyl sulfide (10M, 0.4 mL, 4.0 mmol) in dry THF (6.8 mL) was added at a rate to maintain the internal temperature at -15° C. The solution was stirred at -15° C. for 1 hour then at 22° C. for 6 hours. The product was isolated by the method decribed in Example 34 Step E. The enantiomeric ratio of the purified product was 95:5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05189177 |
| Source dataset | uspto-grants-1993_02 |
| ORD ID | ord-e941b227db9e492291cf9d5d1feca6a1 |
| Source note | uspto-grants-1993_02 |