関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Methyl L-phenylalaninate hydrochloride | HCID 75736 | — |
| 反応物 | (Formyloxy)acetonitrile | HCID 4205685 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2-Benzyl-2-formamidoacetic acid methyl ester | HCID 595529 | — |
反応手順
Cyanomethyl formate (Aldrich, Order No. 453579, 5.05 g, 59.3 mmole) was suspended together with the phenylalanine methyl ester hydrochloride (Aldrich, Order No. 525472, 12.80 g, 59.3 mmole) in 80 ml dichloromethane and cooled to 0° C. in an ice bath. Triethylamine (6.01 g, 59.3 mmole) dissolved in 15 ml of dichloromethane was then added and the mixture was stirred for 16 hours at room temperature. A clear solution formed. In order to work up the mixture the latter was diluted with 100 ml of dichloromethane and washed firstly with 200 ml of saturated NaHCO3 solution and then twice with saturated NaCl solution. The organic phase was dried over magnesium sulfate and concentrated by evaporation. The product obtained was used without further purification for the next stage.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US07608619B2 |
|---|
| 出典データセット | uspto-grants-2009_10 |
|---|
| ORD ID | ord-f55b2bd79a4941678b2e99a6a610d7b7 |
|---|
| 出典メモ | uspto-grants-2009_10 |
|---|