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Dimethyl Succinate → 3-Carbomethoxy-4-(3-methoxyphenyl)-3-butenoic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethyl Succinate | HCID 7820 | — |
| 反応物 | 3-Methoxybenzaldehyde | HCID 11569 | — |
| 反応物 | Potassium tert-butoxide | HCID 23665647 | — |
| 溶媒 | tert-Butanol | HCID 6386 | — |
| 生成物 | 3-Carbomethoxy-4-(3-methoxyphenyl)-3-butenoic acid | HCID 589607 | — |
反応手順
To a refluxing suspension of 15.71 g (140 mmol, 1.4 eq) of potassium t-butoxide in 50 ml of t-butylalcohol is dropped in a mixture of 12.17 (100 mmol) of 3-methoxybenzaldehyde and 15.70 ml (120 mmol, 1.2 eq) of dimethyl succinate dissolved in 20 ml of t-butylalcohol. The mixture is refluxed for 3 hours, concentrated in vacuo, acidified to pH ~1 using 1N HCl, and extracted with ethylacetate. The organics are dried (MgSO4) and concentrated in vacuo to give 3-carbomethoxy-4-(3-methoxyphenyl)-3-butenoic acid in the form of a yellow oil which is used directly in the next step.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05468898 |
| 出典データセット | uspto-grants-1995_11 |
| ORD ID | ord-9dbac76f957c46e69eb4d7b1f14b508a |
| 出典メモ | uspto-grants-1995_11 |