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Ethylmorpholine → N-((Phenylmethoxy)carbonyl)glycine ethyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethylmorpholine | HCID 7525 | — |
| 反応物 | Benzyloxycarbonylglycine | HCID 14349 | — |
| 反応物 | Phosphinic acid, P-ethyl-P-methyl-, P,P'-anhydride | HCID 103894 | — |
| 反応物 | Glycine ethyl ester, hydrochloride | HCID 2723640 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | N-((Phenylmethoxy)carbonyl)glycine ethyl ester | HCID 14366 | — |
反応手順
At 0° C., 7.0 g (0.05 mol) of H-Gly-OC2H5.HCl, 15 ml of N-ethyl morpholine and 20 g of methylethylphosphinic acid anhydride were added successively to a solution of 10.5 g (0.05 mol) of carbobenzoxy-glycine in 20 ml DMF, while stirring and cooling thoroughly. The mixture was brought to room temperature, while stirring. After 16 hours of standing at room temperature the solvent was distilled off in vacuo, and the residue was dissolved in a mixture of 200 ml of ethyl acetate and 100 ml of a 5% potassium bisulfate solution. The ethyl acetate solution was washed twice with 100 ml each of saturated sodium bicarbonate solution, dried over sodium sulfate and evaporated in vacuo.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04426325 |
| 出典データセット | uspto-grants-1984_01 |
| ORD ID | ord-19a090a5a38749ddb70f39e100c2a409 |
| 出典メモ | uspto-grants-1984_01 |