戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 258139作成日:2026年10月27日

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/258139

反応式

関与物質

役割名称HCID仕込み量
反応物7,7-Dioxo-5,6-dihydrothieno[2,3-b]thiopyran-4-oneHCID 3613959—
反応物(Dimethyl sulfide)trihydroboronHCID 12423031—
反応物HCID 178419236HCID 178419236—
溶媒TetrahydrofuranHCID 8028—
生成物(R)-(+)-5,6-Dihydro-4H-thieno[2,3-b]-thiopyran-4-ol-7,7-dioxideHCID 1480164—

反応条件

温度-15 °C

反応手順

To a magnetically stirred solution of 5,6-Dihydro-4H-thieno[2,3-b]-thiopyran-4-one-7,7-dioxide (12) (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 -151° 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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05264585
出典データセットuspto-grants-1993_11
ORD IDord-500a47173bc9456085a5e6d99bb279dc
出典メモuspto-grants-1993_11