홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

2-Chloroethanol → 1-(2-Hydroxy-ethyl)-piperidine-4-carboxylic acid amide

HRID 2414122
노트
인쇄 미리보기

반응식

HRID 2414122 반응식
Cl[CH2:2][CH2:3][OH:4].C(=O)([O-])[O-].[K+].[K+].[I-].[Na+].[C:13]([CH:16]1[CH2:21][CH2:20][NH:19][CH2:18][CH2:17]1)(=[O:15])[NH2:14]>C(O)C>[OH:4][CH2:3][CH2:2][N:19]1[CH2:20][CH2:21][CH:16]([C:13](=[O:15])[NH2:14])[CH2:17][CH2:18]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 342-ChloroethanolHCID 37724-PiperidinecarboxamideHCID 5238Sodium IodideHCID 11430Potassium Carbonate

생성물 1

HCID 28224721-(2-Hydroxy-ethyl)-piperidine-4-carboxylic acid amide

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

2-Chloroethanol (23.9 ml), potassium carbonate (82.0 g) and sodium iodide (4.5 g) were added to an ethanol solution (500 ml) of 4-carbamoylpiperidine (35 g), followed by refluxing for 20 hours. After allowing the reaction mixture to cool down to room temperature, it was filtered through Celite (trade mark). The filtrate was concentrated under reduced pressure. After washing the residue, it was dried to obtain 46.6 g of the desired product.

후처리

  1. temperatureby refluxing for 20 hours
  2. filtrationit was filtered through Celite (trade mark)
  3. concentrationThe filtrate was concentrated under reduced pressure
  4. washAfter washing the residue, it
  5. customwas dried

출처 및 근거

ORD 기록
ord-e56d6e7c8f5f4578b3f97d929bf05aa7
출처 데이터셋
uspto-grants-1988_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04721788

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트