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2-Mercaptoethanol → 4'-(2-Hydroxy-ethylsulfanylmethyl)-biphenyl-2-carboxylic acid ethyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Mercaptoethanol | HCID 1567 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | Ethyl 4'-(bromomethyl)-[1,1'-biphenyl]-2-carboxylate | HCID 46830451 | — |
| 反応物 | 4'-(2-Hydroxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid ethyl ester | HCID 58610579 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 4'-(2-Hydroxy-ethylsulfanylmethyl)-biphenyl-2-carboxylic acid ethyl ester | HCID 58610594 | 42% |
反応手順
4′-(2-Hydroxy-ethylsulfanylmethyl)-biphenyl-2-carboxylic acid ethyl ester was prepared as described for 4′-(2-hydroxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid ethyl ester. 4′-Bromomethyl-biphenyl-2-carboxylic acid ethyl ester (4.1 g, 12.84 mmol, 1 eq.) in anhydrous DMF was treated with 2-mercaptoethanol (1.2 g, 15.41 mmol, 1.2 eq.) and potassium carbonate (5.32 g, 38.52 mmol, 3 eq.). When complete, the reaction was worked up and purified as described for 4′-(2-hydroxy-ethylsulfanylmethyl)-biphenyl4-carboxylic acid ethyl ester to leave 4′-(2-hydroxy-ethylsulfanylmethyl)-biphenyl-2-carboxylic acid ethyl ester (3.05 g, 42% yield) as a light yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07132456B2 |
| 出典データセット | uspto-grants-2006_11 |
| ORD ID | ord-2c769b8dbf7f4965b24ec406c6459a81 |
| 出典メモ | uspto-grants-2006_11 |