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O-Cresol → (E)-3-o-tolyloxy-but-2-enoic acid ethyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | O-Cresol | HCID 335 | — |
| 反応物 | Ethyl 2-butynoate | HCID 78043 | — |
| 反応物 | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (E)-3-o-tolyloxy-but-2-enoic acid ethyl ester | HCID 66894216 | — |
反応手順
To a stirred mixture of 2-methyl-phenol (4.90 g, 0.045 mol) and ethyl-2-butynoate (10.1 g, 0.09 mol) in tetrahydrofuran (15 mL) was added 1,8-diazabicyclo[5.4.0]undec-7-ene (6.80 g, 0.045 mol) slowly. After addition was complete the mixture was stirred at reflux for 6 h. Upon completion of the reaction the tetrahydrofuran was removed in vacuo and the residue was diluted in diethyl ether and washed first with 1N aqueous hydrochloric acid, then 10% aqueous sodium hydroxide solution, a saturated sodium chloride solution and dried over magnesium sulfate. The crude product, (E)-3-o-tolyloxy-but-2-enoic acid ethyl ester, was obtained as a brown oil (6.45 g, 65%) and used without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07741327B2 |
| 出典データセット | uspto-grants-2010_06 |
| ORD ID | ord-d62cd1908464458c8d54b3ca4efbb353 |
| 出典メモ | uspto-grants-2010_06 |