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(2-(Dimethylamino)ethyl)triphenylphosphonium bromide → (E)-3-{6-[3-Dimethylamino-1-(4-tolyl)prop-1E-enyl]-2-pyridyl}acrylic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | (2-(Dimethylamino)ethyl)triphenylphosphonium bromide | HCID 2724136 | — |
| 反応物 | (E)-3-[6-(p-toluoyl)-2-pyridyl]acrylic acid | HCID 11971260 | — |
| 生成物 | (E)-3-{6-[3-Dimethylamino-1-(4-tolyl)prop-1E-enyl]-2-pyridyl}acrylic acid | HCID 13191753 | — |
反応手順
Treatment of (E)-3-[6-(4-toluoyl)-2-pyridyl]acrylic acid, vide supra, with the Wittig reagent derived from triphenyldimethylaminoethylphosphonium bromide by the method of example 1 gave a mixture of isomeric acids which were separated by fractional crystallization from ethyl acetate. The less-soluble E-isomer, (E)-3-{6-[3-dimethylamino-1-(4-tolyl)prop-1E-enyl]-2-pyridyl}acrylic acid was purified by crystallization from isopropanol, m.p. 222°-225° (decomp.)
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04562258 |
| 出典データセット | uspto-grants-1985_12 |
| ORD ID | ord-8d3ddce9407f402e84abec22115d5459 |
| 出典メモ | uspto-grants-1985_12 |