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

HRID 362864
ノート
印刷プレビュー

反応式

HRID 362864 の反応式
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
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 178418647HCID 178418647、化合物触媒HCID 962Water溶媒

実験手順

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.;

後処理

  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

出典と根拠

ORDレコード
ord-d1d46d2ed5a84565a4b8ded541278783
出典データセット
uspto-grants-1999_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05872118

反応ノート

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