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Ethanolamine → Benzyl 4-[(2hydroxyethyl)amino]piperidin-1-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethanolamine | HCID 700 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Benzyl 4-oxopiperidine-1-carboxylate | HCID 643496 | — |
| 反応物 | Sodium triacetoxyborohydride | HCID 5049666 | — |
| 溶媒 | 1,2-Dichloroethane | HCID 11 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | Benzyl 4-[(2hydroxyethyl)amino]piperidin-1-carboxylate | HCID 22137568 | 107.7% |
反応手順
A solution of benzyl 4-oxopiperidin-1-carboxylate (7.0 g), 2-aminoethanol (2.8 g) and acetic acid (2.7 g) in 1,2-dichloroethane (150 mL)-methanol (10 mL) was stirred at room temperature for 3 hours, sodium triacetoxyborohydride (12.7 g) was added thereto, and the mixture was stirred at room temperature for 15 hours. A 1N sodium hydroxide solution was added to the reaction mixture, pH of the aqueous layer was adjusted to about 12, and then the organic layer was separated. The organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure to obtain the title compound (9.0 g, quantitative) as a colorless oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07745623B2 |
| 出典データセット | uspto-grants-2010_06 |
| ORD ID | ord-75db2ba6c6b64dc88b6623abe37c1296 |
| 出典メモ | uspto-grants-2010_06 |