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

Hydrogen Bromide → 1-(6-Hydroxy-2-naphthalenyl)-1-propanone

HRID 2294276
노트
인쇄 미리보기

반응식

HRID 2294276 반응식
C[O:2][C:3]1[CH:12]=[CH:11][C:10]2[C:5](=[CH:6][CH:7]=[C:8]([C:13](=[O:16])[CH2:14][CH3:15])[CH:9]=2)[CH:4]=1.Br>C(O)(=O)C>[C:13]([C:8]1[CH:9]=[C:10]2[C:5](=[CH:6][CH:7]=1)[CH:4]=[C:3]([OH:2])[CH:12]=[CH:11]2)(=[O:16])[CH2:14][CH3:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 260Hydrogen BromideHCID 759131-(6-Methoxy-2-naphthalenyl)-1-propanone

생성물 1

HCID 214748621-(6-Hydroxy-2-naphthalenyl)-1-propanone수율 56.7%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

To a solution of 10 g of 2-methoxy-6-propionylnaphthalene, prepared according to J. Chem. Soc. (1934), p. 864, in acetic acid (45 ml) and kept under reflux, 47 ml of aqueous HBr (48% by weight) is added during a three-hour time period. The resulting suspension is poured onto 500 g of crushed ice; the formed tars are left in the reaction flask. A suspension is obtained which is filtered on a Buchner filter. The solid material is washed with 100 ml of water, 50 ml of saturated aqueous solution of NaHCO3, and then with 50 ml of water. After drying in air and in oven at 60° C. for 10 hours, 5.3 g of pink-white product is obtained with the following characteristics:

후처리

  1. temperatureunder reflux
  2. waitthe formed tars are left in the reaction flask
  3. customA suspension is obtained which
  4. filtrationis filtered on a Buchner
  5. filtrationfilter
  6. washThe solid material is washed with 100 ml of water, 50 ml of saturated aqueous solution of NaHCO3
  7. customAfter drying in air and in oven at 60° C. for 10 hours

출처 및 근거

ORD 기록
ord-e7a1a3b594294f0c9ac18c5194dbfa91
출처 데이터셋
uspto-grants-1997_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05688846

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트