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Benzoyl chloride → Ethyl 3-Oxo-3-phenyl-2-(thiophen-2-yl)propanoate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Benzoyl chloride | HCID 7412 | — |
| 反応物 | Ethyl 2-thienylacetate | HCID 93657 | — |
| 生成物 | Ethyl 3-Oxo-3-phenyl-2-(thiophen-2-yl)propanoate | HCID 67422066 | — |
反応手順
From benzoyl chloride and ethyl 2-(thiophene-2-yl)acetate, the title compound was prepared using a similar method to the one described in Example 1.14, Step A to give a clear oil. 1H NMR (400 M Hz, CDCl3) δ ppm 1.22 (t, J=7.07 Hz, 3H), 4.16-4.26 (m, 2H), 5.88 (s, 1H), 6.96-7.02 (m, 1H), 7.07 (d, J=3.03 Hz, 1H), 7.31 (dd, J=5.18, 1.14 Hz, 1H), 7.46 (t, J=7.71 Hz, 2H), 7.57 (t, J=7.33 Hz, 1H), 7.98-8.02 (m, 2H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08940891B2 |
| 出典データセット | uspto-grants-2015_01 |
| ORD ID | ord-72068dd81efb4b0db3172620e36bd136 |
| 出典メモ | uspto-grants-2015_01 |