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

Sodium borohydride → 6-Fluoro-1,2,3,4-tetrahydronaphthalen-2-ol

HRID 1388588
노트
인쇄 미리보기

반응식

HRID 1388588 반응식
[BH4-].[Na+].[F:3][C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][CH:13]=1)[CH2:10][C:9](=[O:14])[CH2:8][CH2:7]2>C(O)C.C(OCC)(=O)C>[F:3][C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][CH:13]=1)[CH2:10][CH:9]([OH:14])[CH2:8][CH2:7]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 4311764Sodium borohydrideHCID 50443856-Fluoro-1,2,3,4-tetrahydronaphthalen-2-one

생성물 1

HCID 196994886-Fluoro-1,2,3,4-tetrahydronaphthalen-2-ol수율 80%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 8857Ethyl Acetate용매

실험 절차

Sodium borohydride (1.67 g) was added in portions to a solution of 6-fluoro-2-tetralone (6.56 g) in dry ethanol (30 ml) with stirring, keeping the temperature below 25° C. The mixture was then stirred at room temperature for 3 hours. The mixture was then diluted with a little ethyl acetate and concentrated to an oily residue. Dilute sulphuric acid was added dropwise until effervescence no longer occurred. The mixture was extracted with ether and the extract washed, dried, and concentrated to give an oil. This was distilled (b.p. 75-77/0.1 Torr) to give 6-fluorotetralin-2-ol (5.31 g) containing a trace of the tetralone starting material.

후처리

  1. customthe temperature below 25° C
  2. stirringThe mixture was then stirred at room temperature for 3 hours
  3. concentrationconcentrated to an oily residue
  4. additionDilute sulphuric acid was added dropwise until effervescence
  5. extractionThe mixture was extracted with ether
  6. washthe extract washed
  7. customdried
  8. concentrationconcentrated
  9. customto give an oil
  10. distillationThis was distilled (b.p. 75-77/0.1 Torr)

출처 및 근거

ORD 기록
ord-80fcd6266e90474a9d86e62215b9613f
출처 데이터셋
uspto-grants-1984_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04431834

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트