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Hydrochloric Acid → 4-Fluoro-7-hydroxy-2,3-dihydro-1H-inden-1-one

HRID 440831
ノート
印刷プレビュー

反応式

HRID 440831 の反応式
C([O:5][C:6]1[CH:11]=[CH:10][C:9]([F:12])=[CH:8][CH:7]=1)(=O)C=C.[Cl-].[Al+3].[Cl-].[Cl-].[Cl-].[Na+].Cl>>[F:12][C:9]1[CH:8]=[CH:7][C:6]([OH:5])=[C:11]2[C:10]=1[CH2:8][CH2:7][C:6]2=[O:5]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 4

HCID 313Hydrochloric AcidHCID 5234Sodium ChlorideHCID 6451240Aluminum(III) ChlorideHCID 185460004-Fluorophenyl 2-propenoate

生成物 1

HCID 152684884-Fluoro-7-hydroxy-2,3-dihydro-1H-inden-1-one収率 95.8%

反応条件

温度
80 °C

実験手順

4-Fluorophenyl acrylate (12.0 g) was added to a mixture of aluminum chloride (33.7 g) and sodium chloride (14.8 g), and the mixture was stirred at 80° C. for 2 hours and then at 160° C. for 1 hour. After completion of the reaction, ice-water and concentrated hydrochloric acid were added, and the reaction mixture was extracted with chloroform. The extract was washed with a saturated aqueous solution of sodium chloride and dried over magnesium sulfate. The solvent was evaporated, and the resulting residue was purified by silica gel column chromatography. From the eluate of hexane-ethyl acetate (9:1), 4-fluoro-7-hydroxy-1-indanone (5.75 g) was obtained as a pale yellow powder.

後処理

  1. waitat 160° C. for 1 hour
  2. additionwere added
  3. extractionthe reaction mixture was extracted with chloroform
  4. washThe extract was washed with a saturated aqueous solution of sodium chloride
  5. dry with materialdried over magnesium sulfate
  6. customThe solvent was evaporated
  7. customthe resulting residue was purified by silica gel column chromatography

出典と根拠

ORDレコード
ord-61a38ba01aad4f818533352c8b900a7b
出典データセット
uspto-grants-1996_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05521180

反応ノート

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