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

HCID 22492926, 화합물 → HCID 22492895, 화합물

HRID 1816694
노트
인쇄 미리보기

반응식

HRID 1816694 반응식
Br[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][O:7][CH:8]1[CH2:13][CH2:12][N:11]([C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])[CH2:10][CH2:9]1.[CH3:21][OH:22].C[O-].[Na+]>CO>[CH3:21][O:22][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][O:7][CH:8]1[CH2:13][CH2:12][N:11]([C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])[CH2:10][CH2:9]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 22492926HCID 22492926, 화합물HCID 23694274Sodium methanolate methanol

생성물 1

HCID 22492895HCID 22492895, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of 4-(5-bromopentyloxy)-1-N-t-butyloxycarbonylpiperidine (2.44 g) in methanol (13 ml) was added 28% sodium methoxide methanol solution (14.2 ml), and the mixture was stirred under reflux for 4 hours. The reaction mixture was evaporated in vacuo. The resulting residue was chromatographed on silica gel (250 ml) eluting with a mixture of n-hexane and ethyl acetate (5:1 v/v). The fractions containing the object compound were collected and evaporated under reduced pressure to give 4-(5-methoxypentyloxy)-1-N-t-butyloxycarbonylpiperidine (1.97 g).

후처리

  1. temperatureunder reflux for 4 hours
  2. customThe reaction mixture was evaporated in vacuo
  3. customThe resulting residue was chromatographed on silica gel (250 ml)
  4. washeluting with a mixture of n-hexane and ethyl acetate (5:1 v/v)
  5. additionThe fractions containing the object compound
  6. customwere collected
  7. customevaporated under reduced pressure

출처 및 근거

ORD 기록
ord-f170ae24fe89475985bee857ff8db7e1
출처 데이터셋
uspto-grants-2005_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06884868B1

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트