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

(3-((8-(1,3-Dioxolan-2-yl)octyl)oxy)-5-bromophenyl)methanol → 3-((8-(1,3-Dioxolan-2-yl)octyl)oxy)-5-bromobenzaldehyde

HRID 332660
노트
인쇄 미리보기

반응식

HRID 332660 반응식
[O:1]1[CH2:5][CH2:4][O:3][CH:2]1[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][O:14][C:15]1[CH:16]=[C:17]([CH2:22][OH:23])[CH:18]=[C:19]([Br:21])[CH:20]=1.[O-2].[Mg+4].[O-2]>O1CCOCC1>[O:1]1[CH2:5][CH2:4][O:3][CH:2]1[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][O:14][C:15]1[CH:16]=[C:17]([CH:18]=[C:19]([Br:21])[CH:20]=1)[CH:22]=[O:23]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 71093288(3-((8-(1,3-Dioxolan-2-yl)octyl)oxy)-5-bromophenyl)methanol

생성물 1

HCID 866769003-((8-(1,3-Dioxolan-2-yl)octyl)oxy)-5-bromobenzaldehyde수율 74.4%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

반응 조건

온도
100 °C

실험 절차

To a stirred solution of (3-((8-(1,3-dioxolan-2-yl)octyl)oxy)-5-bromophenyl)methanol (1.69 g, 4.36 mmol) in 1,4-dioxane (25 mL), was added magnesium (IV) oxide (1.90 g, 21.9 mmol). The reaction mixture was heated to 100° C. for 16 hours. The suspension was filtered, washed with ethyl acetate, and the filtrate was concentrated under reduced pressure to afford the title compound (1.25 g, 74%).

후처리

  1. filtrationThe suspension was filtered
  2. washwashed with ethyl acetate
  3. concentrationthe filtrate was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-8c0c932ac45544cc95f7ed432e80f9af
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08877774B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트