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HRID 33794作成日:2026年10月26日

Oxygen → Thianthren-1-ol

https://huagongshe.com/reaction/33794

反応式

関与物質

役割名称HCID仕込み量
反応物OxygenHCID 977—
反応物ThianthreneHCID 7109—
反応物HCID 178418306HCID 178418306—
反応物HCID 178461630HCID 178461630—
溶媒TetrahydrofuranHCID 8028—
生成物Thianthren-1-olHCID 2156943036%

反応手順

To a cooled (−78° C.) solution of thianthrene (10 g, 46.23 mmol) in anhydrous THF (200 ml) was added t-BuLi (1.7M in pentane, 40.81 ml, 69.34 mmol), under a nitrogen atmosphere, over a period of 10 minutes and the resulting yellow solution was then allowed to warm to room temperature and stirred vigorously for a further 16 hours. EtMgBr (3M in THF, 23 ml, 69.34 mmol) was then added in a dropwise fashion to the cooled (0° C.) reaction mixture which was then stirred for a further 45 minutes before oxygen was bubbled through the solution. After two hours the reaction was quenched by dropwise addition of 1M NaOH (100 ml) and washed with EtOAc (1×300 ml) before being acidified to pH4 with aqueous 1M HCl. The mixture was then extracted with EtOAc (3×100 mL),dried (MgSO4), filtered and concentrated in vacuo to give a mild amber slurry that was purified by flash chromatography (SiO2) (10:1, Ethyl acetate/Hexanes), to give the title compound (3.82 g, 36%) as a yellow solid. m/z (LC-MS, ESP):, RT=4.62 min, (M++1)=231

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07429660B2
出典データセットuspto-grants-2008_09
ORD IDord-76a248e004c4433f8e5b089409fa7051
出典メモuspto-grants-2008_09