Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Ethanolamine → Benzyl 4-[(2hydroxyethyl)amino]piperidin-1-carboxylate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Ethanolamine | HCID 700 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Benzyl 4-oxopiperidine-1-carboxylate | HCID 643496 | — |
| 반응물 | Sodium triacetoxyborohydride | HCID 5049666 | — |
| 용매 | 1,2-Dichloroethane | HCID 11 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | Benzyl 4-[(2hydroxyethyl)amino]piperidin-1-carboxylate | HCID 22137568 | 107.7% |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07745623B2 |
| 출처 데이터셋 | uspto-grants-2010_06 |
| ORD ID | ord-75db2ba6c6b64dc88b6623abe37c1296 |
| 출처 메모 | uspto-grants-2010_06 |