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Nitric Acid → 4,5-Dimethoxy-2-nitrophenol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Nitric Acid | HCID 944 | — |
| 反応物 | 3,4-Dimethoxyphenol | HCID 16251 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 生成物 | 4,5-Dimethoxy-2-nitrophenol | HCID 297121 | — |
反応手順
In SCHEME 9 3,4-dimethoxyphenol (36) is selectively nitrated with 70% HNO3 in AcOH to give 4,5-dimethoxy-2-nitrophenol (37) which is further converted to the corresponding triflate (38) with trifluoromethylsulfonic anhydride (Tf2O) and pyridine in dichloromethane. Triflate (38) is reacted under inert conditions with a boronic acid of general type (31) under Suzuki-type basic conditions (Pd(PPh3)4 and aqueous potassium phosphate in toluene) to a biaryl of type (39). Biaryl (39) is further hydrolized with aqueous lithium hydroxide in THF and MeOH or MeCN to give the corresponding carboxylic acid (40) which is converted to a building block of type (41) by reaction with oxalyl chloride in anhydrous dichloromethane.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07851501B2 |
| 出典データセット | uspto-grants-2010_12 |
| ORD ID | ord-470721f2c58e44d09b9fdde48812aa67 |
| 出典メモ | uspto-grants-2010_12 |