Hydrochloric Acid → 4-[3-(3-Acetoxy-4-acetyl-2-propylphenoxy)propoxy]-3-bromobenzoic acid

HRID 986705ノート

反応式

HRID 986705 の反応式
[C:1]([O:4][C:5]1[C:6]([CH2:33][CH2:34][CH3:35])=[C:7]([CH:27]=[CH:28][C:29]=1[C:30](=[O:32])[CH3:31])[O:8][CH2:9][CH2:10][CH2:11][O:12][C:13]1[CH:25]=[CH:24][C:16]([C:17]([O:19]C(C)(C)C)=[O:18])=[CH:15][C:14]=1[Br:26])(=[O:3])[CH3:2].Cl>O1CCOCC1>[C:1]([O:4][C:5]1[C:6]([CH2:33][CH2:34][CH3:35])=[C:7]([CH:27]=[CH:28][C:29]=1[C:30](=[O:32])[CH3:31])[O:8][CH2:9][CH2:10][CH2:11][O:12][C:13]1[CH:25]=[CH:24][C:16]([C:17]([OH:19])=[O:18])=[CH:15][C:14]=1[Br:26])(=[O:3])[CH3:2]

参加物

4

反応物 2

HCID 313Hydrochloric Acid2 回HCID 20157030Tert-butyl 4-[3-(3-acetoxy-4-acetyl-2-propylphenoxy)propoxy]-3-bromobenzoate

生成物 1

HCID 137456304-[3-(3-Acetoxy-4-acetyl-2-propylphenoxy)propoxy]-3-bromobenzoic acid収率 26%

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒3 回

実験手順

To a solution of tert-butyl 4-[3-(3-acetoxy-4-acetyl-2-propylphenoxy)propoxy]-3-bromobenzoate (1.5 g) in dioxane (10 ml) was added a cooled solution of 2 N hydrogen chloride in dioxane (10 ml) at 20° C. under stirring. The reaction mixture was warmed to room temperature, and stirred for 30 minutes. To the mixture was added an additional cooled solution of 2 N hydrogen chloride in dioxane (10 ml). The mixture was stirred for 1.5 hours and subjected to concentration under reduced pressure. The residue was dissolved in chloroform (30 ml), and the solution was washed with water (30 ml) and dried with magnesium sulfate. The solvent was removed by evaporation, and the residue was dissolved in isopropyl ether. The solution was treated with activated carbon, and to the solution was added hexane to give crystals. The crystals were collected by filtration, subjected to silica gel column chromatography, and subjected to recrystallization from aqueous ethanol to give colorless crystals of 4-[3-(3-acetoxy-4-acetyl-2-propylphenoxy)propoxy]-3-bromobenzoic acid (0.35 g). M.p. 154°-156° C.

後処理

  1. stirringstirred for 30 minutes
  2. stirringThe mixture was stirred for 1.5 hours
  3. concentrationsubjected to concentration under reduced pressure
  4. dissolutionThe residue was dissolved in chloroform (30 ml)
  5. washthe solution was washed with water (30 ml)
  6. dry with materialdried with magnesium sulfate
  7. customThe solvent was removed by evaporation
  8. dissolutionthe residue was dissolved in isopropyl ether
  9. additionThe solution was treated with activated carbon
  10. additionto the solution was added hexane
  11. customto give crystals
  12. filtrationThe crystals were collected by filtration
  13. customsubjected to recrystallization from aqueous ethanol

出典と根拠

ORDレコード
ord-0d84a2936521490c904bb8da3a0c2159
出典データセット
uspto-grants-1987_12
特許番号
US04714774

反応ノート

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