関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Tert-Butyl nitrite | HCID 10906 | — |
| 反応物 | Dimethyl Disulfide | HCID 12232 | — |
| 反応物 | (3-Amino-5-(trifluoromethyl)phenyl)methanol | HCID 53414333 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | [3-(Methylthio)-5-(trifluoromethyl)phenyl]methanol | HCID 68687257 | — |
反応手順
To a solution of [3-amino-5-(trifluoromethyl)phenyl]methanol (319 mg, 1.67 mmol) (Step A, Example 24) in CHCl3 (5 mL) was added dimethyl disulfide (296 μL, 3.34 mmol). Next, t-butyl nitrite (285 μL, 2.4 mmol) was added dropwise by syringe. The reaction was stirred at room temperature for two hours and then poured into H2O (15 mL). The mixture was extracted with EtOAc (50 mL), washed with brine (15 mL), dried over Na2SO4, filtered, and concentrated. Purification by flash chromatography with 0% to 50% EtOAc/hexanes afforded [3-(methylthio)-5-(trifluoromethyl)phenyl]-methanol. The [3-(methylthio)-5-(trifluoromethyl)phenyl]methanol was contaminated with minor impurities that were removed after the next step. Rf=0.53 (50% EtOAc/hexanes). 1H NMR (CDCl3, 500 MHz) δ 7.63 (s, 1H), 7.40 (s, 1H), 7.35 (s, 1H), 4.71 (s, 2H), 2.51 (s, 3H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07737295B2 |
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| 出典データセット | uspto-grants-2010_06 |
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| ORD ID | ord-1da571ec2709469d8671e84f4069c2ac |
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| 出典メモ | uspto-grants-2010_06 |
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