化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1743260作成日:2026年10月27日
Ammonium Chloride → Tert-butyl (3r,5r,6s)-2-oxo-5,6-diphenyl-3-[1-(2-trimethylsilanyl-ethoxycarbonyl)piperidin-4-yl]morpholine-4-carboxylate
https://huagongshe.com/reaction/1743260
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | 15-Crown-5 | HCID 36336 | — |
| 反応物 | tert-butyl (2R,3S)-6-oxo-2,3-diphenylmorpholine-4-carboxylate | HCID 981230 | — |
| 反応物 | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| 反応物 | 2-Trimethylsilanylethyl 4-iodopiperidine-1-carboxylate | HCID 22238408 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Tert-butyl (3r,5r,6s)-2-oxo-5,6-diphenyl-3-[1-(2-trimethylsilanyl-ethoxycarbonyl)piperidin-4-yl]morpholine-4-carboxylate | HCID 90791180 | — |
反応手順
4 g of tert-butyl (5S,6R)-2-oxo-5,6-diphenylmorpholine-4-carboxylate were dissolved in 50 ml of THF. 9 ml of 15-crown-5 were added, and the mixture was cooled to −78° C. Then 6.8 ml of a 2 M solution of NaHMDS in THF were added dropwise. The mixture was stirred for 10 min and then 8 g of 2-trimethylsilanylethyl 4-iodopiperidine-1-carboxylate were added dropwise. The mixture was allowed to warm to 0° C. over the course of 6 h, and then the reaction was stopped by adding 200 ml of saturated ammonium chloride solution. The aqueous phase was extracted 3 times with 150 ml of ethyl acetate each time, and the combined organic phases were dried with MgSO4. The solvents were removed in vacuo, and the residue was chromatographed on silica gel.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US07008957B2 |
|---|
| 出典データセット | uspto-grants-2006_03 |
|---|
| ORD ID | ord-3e41b89821224680bb8e0715a9e0af01 |
|---|
| 出典メモ | uspto-grants-2006_03 |
|---|