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1,2-Dimethoxyethane → 3-Hydroxy-6-fluoro-1-indanone

HRID 362864
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HRID 362864 반응식
Br[CH:2]1[C:10]2[C:5](=[CH:6][C:7]([F:11])=[CH:8][CH:9]=2)[C:4](=[O:12])[CH2:3]1.C(COC)[O:14]C>O.C(=O)([O-])[O-].[Ag+2]>[OH:14][CH:2]1[C:10]2[C:5](=[CH:6][C:7]([F:11])=[CH:8][CH:9]=2)[C:4](=[O:12])[CH2:3]1
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참가 물질

5

반응물 2

HCID 80711,2-DimethoxyethaneHCID 232936813-Bromo-6-fluoro-1-indanone

생성물 1

HCID 232935953-Hydroxy-6-fluoro-1-indanone

시약·촉매·용매 2

HCID 178418647HCID 178418647, 화합물촉매HCID 962Water용매

실험 절차

A mixture of 3-bromo-6-fluoro-1-indanone (2.50 g, 10.0 mmoles) and silver carbonate (4.19 g, 15.2 mmoles, Aldrich) in dimethoxyethane (85 mL) and water (65 mL) was stirred overnight at ambient temperature. The mixture was filtered through a pad of celite, and the filtrate was diluted with water (500 mL) and extracted with ethyl acetate (4×100 mL). The combined extracts were washed with water (100 mL) and brine (75 mL), dried over sodium sulfate, filtered, and evaporated in vacuo to give 2.80 g (quantitative) of crude 3-hydroxy-6-fluoro-1-indanone which was used without further purification. Chromatography of 0.41 g on silica gel, eluting with hexane: ethyl acetate (3:4) gave 0.050 g of analytically pure 3-hydroxy-6-fluoro-1-indanone as a tan solid, mp 73°-76° C.;

후처리

  1. filtrationThe mixture was filtered through a pad of celite
  2. additionthe filtrate was diluted with water (500 mL)
  3. extractionextracted with ethyl acetate (4×100 mL)
  4. washThe combined extracts were washed with water (100 mL) and brine (75 mL)
  5. dry with materialdried over sodium sulfate
  6. filtrationfiltered
  7. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-d1d46d2ed5a84565a4b8ded541278783
출처 데이터셋
uspto-grants-1999_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05872118

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