関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Vanillin | HCID 1183 | — |
| 反応物 | Dimethylsulphamoyl chloride | HCID 83372 | — |
| 反応物 | Ethyl acetate hexane | HCID 21226206 | — |
| 溶媒 | N,N-Dimethylcyclohexylamine | HCID 7415 | — |
| 溶媒 | Hexane | HCID 8058 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 4-(N,N-Dimethylsulfamoyl)-3-methoxybenzaldehyde | HCID 21976871 | — |
反応手順
To a solution of vanillin (4.56 g, 30 mmol) in N,N-dimethylcyclohexylamine (30 mL) at 80-90° C., was added N,N-dimethylsulfamoyl chloride (3.79 mL, 35.27 mmol). The mixture was stirred at this temperature for 4 h, transferred to a separating funnel and diluted with EtOAc (100 mL). The organic layer was washed with water (2×200 mL), 6M HCl (aq.) (200 mL), brine (2×200 mL), dried (Na2SO4) and filtered. Concentration in vacuo of the combined filtrates gave a golden-yellow oil which solidified on standing. The product was stirred in n-hexane, filtered and air-dried to give OBS02011 as yellow plates (6.92 g, 89%). TLC [SiO2, EtOAc-n-hexane (1:1)] Rf=0.65; 1H-NMR (270 MHz, CDCl3)=2.98 (6H, s), 3.93 (3H, s), 7.44 (1H, d, J=1.6), 7.48 (1H, dd, J=1.6, 8.1), 7.53 (1H, d, J=8.1), 9.92 (1H, s).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07745472B2 |
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| 出典データセット | uspto-grants-2010_06 |
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| ORD ID | ord-c05a971138724dfeb0aba79d83b73319 |
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| 出典メモ | uspto-grants-2010_06 |
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