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

1,4-Dihydroxy-2-naphthoic acid → 1-Hydroxy-4-(beta,gamma-dibromopropyloxy)-2-naphthoic acid

HRID 848575
노트
인쇄 미리보기

반응식

HRID 848575 반응식
[OH:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([OH:12])=[CH:4][C:3]=1[C:13]([OH:15])=[O:14].[Br:16][CH:17]([CH2:20][Br:21])[CH2:18]O>>[OH:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([O:12][CH2:18][CH:17]([Br:16])[CH2:20][Br:21])=[CH:4][C:3]=1[C:13]([OH:15])=[O:14]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 6711,4-Dihydroxy-2-naphthoic acidHCID 72812,3-Dibromo-1-propanol

생성물 1

HCID 205655531-Hydroxy-4-(beta,gamma-dibromopropyloxy)-2-naphthoic acid수율 35%

반응 조건

온도
90 °C

실험 절차

60 g (0.3 mol) of 1,4-dihydroxy-2-naphthoic acid was added to 150 ml of 2,3-dibromopropanol and, under heating at 90° C. with stirring, hydrogen chloride gas was bubbled in the mixture during a reaction period of 2 hours. The mixture was cooled to 10° to 20° C. and the crystals precipitated were collected by filteration to obtain 42.4 g (35% yield) of 1-hydroxy-4-(β,γ-dibromopropyloxy)-2-naphthoic acid.

후처리

  1. customhydrogen chloride gas was bubbled in the mixture during a reaction period of 2 hours
  • temperatureThe mixture was cooled to 10° to 20° C.
  • customthe crystals precipitated
  • customwere collected by filteration
  • 출처 및 근거

    ORD 기록
    ord-871727e329864f6f9d3d0279cb7bc2d2
    출처 데이터셋
    uspto-grants-1981_10
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04296200

    반응 노트

    불러오는 중…

    이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트