2-丁基-3-(3,5-二碘-4-羟基苯甲酰)苯并呋喃

反应条件: temp:50.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: A mixture of 2-n-butyl-3-(3,5-diiodo-4-hydroxybenzoyl)benzofuran 1.0 g (1.83 mmol) and potassiumcarbonate 0.56 g (4 mmol) in aceton (dry) 100 ml, α-brom ethylacetate 1.0 g (12 mmol was added, and the solution was extracted with 100 ml water. The organic layer was evaporated to dryness and the yellow rest was dissolved in methanol 50 ml+1M NaOH 50 ml. The solution was heated to 50° C. for 15 h, extracted with 3×75 ml dichloromethane, and dried (MgSO4). Evaporating the solution and purification on silica gave 0.55 g (005). was added the solution was extracted with 100 ml water The organic layer was evaporated to dryness the yellow rest was dissolved in methanol 50 ml+1M NaOH 50 ml extracted with 3×75 ml dichloromethane dried (MgSO4) Evaporating the solution and purification on silica

反应条件: temp:50.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: A mixture of 2-n-butyl-3-(3,5-diiodo-4-hydroxybenzoyl)benzofuran 1.0 g (1.83 mmol) and potassiumcarbonate 0.56 g (4 mmol) in aceton (dry) 100 ml, α-brom ethylacetate 1.0 g (12 mmol) was added, and the solution was extracted with 100 ml water. The organic layer was evaporated to dryness and the yellow rest was dissolved in methanol 50 ml+1M NaOH 50 ml. The solution was heated to 50° C. for 15 h, extracted with 3×75 ml dichloromethane, and dried (MgSO4). Evaporating the solution and purification on silica gave 0.55 g (005). was added the solution was extracted with 100 ml water The organic layer was evaporated to dryness the yellow rest was dissolved in methanol 50 ml+1M NaOH 50 ml extracted with 3×75 ml dichloromethane dried (MgSO4) Evaporating the solution and purification on silica

反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: 32.8 g (60 mmol) of 2-butyl-3-[3,5-diiodo-4-hydroxybenzoyl]benzofuran and 13.8 g (100 mmol) of anhydrous potassium carbonate are initially introduced into 200 ml of acetonitrile. 17.6 g (90 mmol) of ethyl 4-bromobutyrate are added dropwise at room temperature within the space of 30 minutes and the suspension is subsequently heated under reflux for 14 h. Once the reaction solution has been cooled down to room temperature, 200 ml of distilled water are added and the mixture is extracted 3 times with 100 ml of methyl tert-butyl ether. The combined organic extracts are dried and concentrated to dryness. The residue, which consists of 2-butyl-3-[3,5-diiodo-4-(3-ethoxycarbonyl-propyloxy)benzoyl]benzofuran, is introduced into 100 ml of isopropanol and a solution of 39.6 g (600 mmol) of 85% potassium hydroxide in 400 ml of distilled water is added. The suspension is heated at about 60° C. until a clear solution is formed. Once the solution has been cooled down to room temperature, 100 ml of 1N hydrochloric acid are added, and the mixture is adjusted to pH 3 with 32% hydrochloric acid while cooling, and then extracted 3 times with 200 ml of MTB ether on each occasion. The combined organic, dried, rotary-evaporated extracts are taken up in 50 ml of dichloromethane and left at 0° C. for several hours. The pale brown crystals which have precipitated out are stirred up with a further 50 ml of dichloromethane. After filtering with suction, washing and drying, 5.7 g (20%) of almost colourless crystals of 2-butyl-3-[3,5-diiodo-4-(3-carboxypropyloxy)-benzoyl]benzofuran are obtained which can, if desired, be further purified on a silica gel column (MTB ether/methanol=9:1). the suspension is subsequently heated under reflux for 14 h the mixture is extracted 3 times with 100 ml of methyl tert-butyl ether The combined organic extracts are dried concentrated to dryness is introduced into 100 ml of isopropanol The suspension is heated at about 60° C. until a clear solution is formed Once the solution has been cooled down to room temperature while cooling extracted 3 times with 200 ml of MTB ether on each occasion The combined organic, dried rotary-evaporated extracts left at 0° C. for several hours The pale brown crystals which have precipitated out After filtering with suction washing drying

反应条件: temp:50.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: A mixture of 2-n-butyl-3-(3,5-diiodo-4-hydroxybenzoyl)benzofuran 1.0 g (1.83 mmol) and potassiumcarbonate 0.56 g (4 mmol) in aceton (dry) 100 ml, α-brom ethylacetate 1.0 g (12 mmol was added, and the solution was extracted with 100 ml water. The organic layer was evaporated to dryness and the yellow rest was dissolved in methanol 50 ml+1M NaOH 50 ml. The solution was heated to 50° C. for 15 h, extracted with 3×75 ml dichloromethane, and dried (MgSO4). Evaporating the solution and purification on silica gave 0.55 g (005). was added the solution was extracted with 100 ml water The organic layer was evaporated to dryness the yellow rest was dissolved in methanol 50 ml+1M NaOH 50 ml extracted with 3×75 ml dichloromethane dried (MgSO4) Evaporating the solution and purification on silica

反应条件: temp:50.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: A mixture of 2-n-butyl-3-(3,5-diiodo-4-hydroxybenzoyl)benzofuran 1.0 g (1.83 mmol) and potassiumcarbonate 0.56 g (4 mmol) in aceton (dry) 100 ml, α-brom ethylacetate 1.0 g (12 mmol) was added, and the solution was extracted with 100 ml water. The organic layer was evaporated to dryness and the yellow rest was dissolved in methanol 50 ml+1M NaOH 50 ml. The solution was heated to 50° C. for 15 h, extracted with 3×75 ml dichloromethane, and dried (MgSO4). Evaporating the solution and purification on silica gave 0.55 g (005). was added the solution was extracted with 100 ml water The organic layer was evaporated to dryness the yellow rest was dissolved in methanol 50 ml+1M NaOH 50 ml extracted with 3×75 ml dichloromethane dried (MgSO4) Evaporating the solution and purification on silica