関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetic Acid | HCID 176 | — |
| 反応物 | Water | HCID 962 | — |
| 反応物 | Sodium borohydride | HCID 4311764 | — |
| 反応物 | 5-[4-(2-Hydroxy-2-phenylethoxy)benzylidene]-1,3-thiazolidine-2,4-dione | HCID 86645070 | — |
| 触媒 | Dichlorocobalt hexahydrate | HCID 517166 | — |
| 触媒 | Dimethylglyoxime | HCID 135459645 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Sodium Hydroxide | HCID 14798 | — |
| 生成物 | 5-[4-(2-Hydroxy-2-phenylethoxy)benzyl]-1,3-thiazolidine-2,4-dione | HCID 46911041 | 76.3% |
反応手順
To a mixture of 5-[4-(2-hydroxy-2-phenylethoxy)benzylidene]-1,3-thiazolidine-2,4-dione (1.50 g, 4.39 mmol) in THF (20 ml) was added H2O (20 ml), 1M NaOH (3 ml), cobalt (II) chloride hexahydrate (0.60 mg, 0.003 mmol) and dimethylglyoxime (15 mg, 0.13 mmol). A solution of sodium tetrahydroborate (240 mg, 6.33 mmol) in 0.2M NaOH (3.6 ml) was added. The reaction mixture immediately turned dark but very soon assumed a clear yellow appearance. Acetic acid was added dropwise until the solution turned dark (3 drops). After ca. one hour the reaction lightened. Additional NaBH4, CoCl2 and HOAc were added to produce a deep blue-purple color. When that color faded, more NaBH4 was added. When HPLC analysis indicated that the reaction was complete, it was partitioned between H2O and EtOAc, and the organic phase was washed with brine, dried (Na2SO4), filtered and evaporated in vacuo. The resulting foamy solid was chromatographed, eluting with 50% EtOAc/hexanes. Fractions containing product were combined and evaporated in vacuo to give 1.15 g (76%) of the title compound as a white solid. MS (ESI−) for C18H17NO4S m/z 342.1 (M−H)−.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08067450B2 |
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| 出典データセット | uspto-grants-2011_11 |
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| ORD ID | ord-39b815670880479fad523fd465ba821e |
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| 出典メモ | uspto-grants-2011_11 |
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