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

Water → 3,4-dihydro-6,7-dimethoxy-1-isopropyl-2(1H)-naphthalenone

HRID 2118763
노트
인쇄 미리보기

반응식

HRID 2118763 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][C:12]=1[O:13][CH3:14])[CH2:9][C:8](=[O:15])[CH2:7][CH2:6]2.[CH:16](I)([CH3:18])[CH3:17].O>CN(C)C=O>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][C:12]=1[O:13][CH3:14])[CH:9]([CH:16]([CH3:18])[CH3:17])[C:8](=[O:15])[CH2:7][CH2:6]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 6362Isopropyl iodideHCID 6098446,7-Dimethoxy-2-tetralone

생성물 1

HCID 201932173,4-dihydro-6,7-dimethoxy-1-isopropyl-2(1H)-naphthalenone

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

22.0 g of 3,4-dihydro-6,7-dimethoxy-2(1H)-naphthalenone were dissolved in 300 ml of dimethylformamide and treated with 13 g of potassium tert.-butylate. The solution was stirred at 18° for 30 minutes. After the addition of 19.7 g of isopropyl iodide the mixture was stirred for a further 30 minutes, whereby the temperature was held below 30°, and then poured into water. The product was extracted with ether, the extract was washed with water, dried over magnesium sulfate and evaporated. The oil which remained behind was purified by column chromatography (silica gel, hexane/ethyl acetate 6:1). There was obtained 3,4-dihydro-6,7-dimethoxy-1-isopropyl-2(1H)-naphthalenone, m.p. 77°-79°.

후처리

  1. stirringwas stirred for a further 30 minutes
  2. customwas held below 30°
  3. extractionThe product was extracted with ether
  4. washthe extract was washed with water
  5. dry with materialdried over magnesium sulfate
  6. customevaporated
  7. custombehind was purified by column chromatography (silica gel, hexane/ethyl acetate 6:1)

출처 및 근거

ORD 기록
ord-f1ff44d08042418d8a29d8756096b2f6
출처 데이터셋
uspto-grants-1987_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04680310

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트