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

3-Bromophenetole → (1RS,2RS,4SR)-4-(cyclopentylethyl)-2-dimethylaminomethyl-1-(3-ethoxyphenyl)-cyclohexanol hydrochloride

HRID 2392766
노트
인쇄 미리보기

반응식

HRID 2392766 반응식
[ClH:1].[CH:2]1([CH2:7][CH2:8][CH:9]2[CH2:14][CH2:13][C:12](=[O:15])[CH:11]([CH2:16][N:17]([CH3:19])[CH3:18])[CH2:10]2)[CH2:6][CH2:5][CH2:4][CH2:3]1.Br[C:21]1[CH:26]=[CH:25][CH:24]=[C:23]([O:27][CH2:28][CH3:29])[CH:22]=1>>[ClH:1].[CH:2]1([CH2:7][CH2:8][CH:9]2[CH2:14][CH2:13][C:12]([C:21]3[CH:26]=[CH:25][CH:24]=[C:23]([O:27][CH2:28][CH3:29])[CH:22]=3)([OH:15])[CH:11]([CH2:16][N:17]([CH3:19])[CH3:18])[CH2:10]2)[CH2:3][CH2:4][CH2:5][CH2:6]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 758673-BromophenetoleHCID 189804134-(2-Cyclopentyl-ethyl)-2-dimethylaminomethyl-cyclohexanone hydrochloride

생성물 1

HCID 67642001(1RS,2RS,4SR)-4-(cyclopentylethyl)-2-dimethylaminomethyl-1-(3-ethoxyphenyl)-cyclohexanol hydrochloride수율 52%

실험 절차

The base of compound (56) was reacted with 1-bromo-3-ethoxy-benzene corresponding to the conditions described in Example 1. The base obtained was purified with diisopropyl ether via a silica gel column and was taken up in 2-butanone/ether. After adding trimethylchlorosilane/water, compound (58) was obtained in a yield of 52% theoretical.

후처리

  1. customThe base obtained
  2. custom
was purified with diisopropyl ether via a silica gel column
  • additionAfter adding trimethylchlorosilane/water
  • 출처 및 근거

    ORD 기록
    ord-5703f94db2e5419c85bcb4823a696efd
    출처 데이터셋
    uspto-grants-1998_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05801201

    반응 노트

    불러오는 중…

    이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트