化工社化工社 化学情報印刷レポート · 研究参考用
Dichloromethane → N-benzyl-O-benzyl-D-serinamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dichloromethane | HCID 6344 | — |
| 反応物 | Trifluoroacetic acid | HCID 6422 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | N-benzyl-O-benzyl-N2-Boc-D-serinamide | HCID 7216909 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | N-benzyl-O-benzyl-D-serinamide | HCID 67082833 | 90.1% |
反応手順
To a solution of N-benzyl-O-benzyl-N2-Boc-D-serinamide (30 g) and dichloromethane (150 mL), trifluoroacetic acid (150 mL) was added. The solution was stirred for 2 hours at room temperature for completion of reaction. The solution was concentrated under vacuum to obtain solid which was dissolved in water. The aqueous layer was basified to pH 8-10 with 5% sodium hydroxide. The aqueous layer was extracted with ethyl acetate and the combined organic layers washed with brine solution. Organic layer was concentrated under vacuum to obtain an oily residue solidify by n-Hexane to give 20 g of N-benzyl-O-benzyl-D-serinamide.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08853439B2 |
| 出典データセット | uspto-grants-2014_10 |
| ORD ID | ord-be2f9f7a3be14f24980bc1a11043ee1e |
| 出典メモ | uspto-grants-2014_10 |