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

Thionyl Chloride → 1-{2-[4-(Chloro-ethyl)-phenoxy]-ethyl}-piperidine

HRID 2417262
노트
인쇄 미리보기

반응식

HRID 2417262 반응식
[N:1]1([CH2:7][CH2:8][O:9][C:10]2[CH:15]=[CH:14][C:13]([CH2:16][CH2:17]O)=[CH:12][CH:11]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.S(Cl)([Cl:21])=O>C1COCC1>[Cl:21][CH2:17][CH2:16][C:13]1[CH:14]=[CH:15][C:10]([O:9][CH2:8][CH2:7][N:1]2[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]2)=[CH:11][CH:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 22633982HCID 22633982, 화합물

생성물 1

HCID 545605911-{2-[4-(Chloro-ethyl)-phenoxy]-ethyl}-piperidine수율 92%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

2-[4-(2-Piperidin-1-yl-ethoxy)-phenyl]-ethanol (4.23 g, 16.98 mmol) was dissolved in 200 ml of THF. HCl gas was bubbled through the solution at 0° C. for 5 minutes. Still at 0° C. the thionyl chloride (2.48 ml, 33.9 mmol) was added dropwise. The reaction mixture was heated at reflux for 2 hours before it was concentrated. 1-{2-[4-(Chloro-ethyl)-phenoxy]-ethyl}-piperidine (4.74 g, 15.6 mmol) was isolated as a brown semisolid; Yield 92%; MS: 268.3 (M+H)+

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. customHCl gas was bubbled through the solution at 0° C. for 5 minutes
  2. temperatureThe reaction mixture was heated
  3. temperatureat reflux for 2 hours before it
  4. concentrationwas concentrated

출처 및 근거

ORD 기록
ord-ad8d370f18904ece8d9a0df08c58fab5
출처 데이터셋
uspto-grants-2004_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06825354B2

반응 노트

불러오는 중…