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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2248436Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/2248436

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt7,7-Dioxo-5,6-dihydrothieno[2,3-b]thiopyran-4-oneHCID 3613959—
Edukt(Dimethyl sulfide)trihydroboronHCID 12423031—
Edukt(S)-DiphenylprolinolHCID 53249241—
EduktHCID 178419238HCID 178419238—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(R)-(+)-5,6-Dihydro-4H-thieno[2,3-b]-thiopyran-4-ol-7,7-dioxideHCID 1480164—

Reaktionsbedingungen

Temperatur-15 °C

Reaktionsschritte

To a magnetically stirred solution of 5,6-Dihydro-4H-thieno[2,3-b]-thiopyran-4-one-7,7-dioxide (9) (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-methyl 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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05039802
Quelldatensatzuspto-grants-1991_08
ORD IDord-5abd2ed7764e4483af0149dcc4d2517c
Quellennotizuspto-grants-1991_08