反応 #725437

反応方程式

4-(4-hydroxyphenyl)pentanol

potassium carbonate

methyl 3-bromomethyl-2-thiophenecarboxylate

→

product

収率 75.7%

4-[4-(2-Carbomethoxy-3-thienylmethoxy)phenyl]pentanol

収率 75.7%

溶媒

2-butanone

反応条件

後処理

1. 1
   温度was heated
2. 2
   温度under reflux overnight, with exclusion of moisture
3. 3
   ろ過The mixture was filtered while hot and the filter cake
4. 4
   洗浄was washed with 2-butanone
5. 5
   濃縮The combined filtrate was concentrated
6. 6
   洗浄a solution of the residue and dichloromethane was washed with 10% sodium hydroxide solution, water and saturated brine
7. 7
   乾燥The dried (over anhydrous sodium sulfate) organic phase
8. 8
   ろ過was filtered
9. 9
   濃縮the filtrate was concentrated to an oil
10. 10
    その他Purification by high-pressure liquid chromatography (Waters Associates Prep LC/System 500A; two silica gel columns; 0.2 l/min flow rate; Gow Mac model 80-800 UV detector; 30% V/V ethyl acetate in hexane)

実験手順

A stirred suspension of 8.0 g of 4-(4-hydroxyphenyl)pentanol, 18.41 g of anhydrous potassium carbonate, 0.4 g of potassium iodide, 10.44 g of methyl 3-bromomethyl-2-thiophenecarboxylate, and 225 ml of 2-butanone was heated under reflux overnight, with exclusion of moisture. The mixture was filtered while hot and the filter cake was washed with 2-butanone. The combined filtrate was concentrated, and a solution of the residue and dichloromethane was washed with 10% sodium hydroxide solution, water and saturated brine. The dried (over anhydrous sodium sulfate) organic phase was filtered and the filtrate was concentrated to an oil. Purification by high-pressure liquid chromatography (Waters Associates Prep LC/System 500A; two silica gel columns; 0.2 l/min flow rate; Gow Mac model 80-800 UV detector; 30% V/V ethyl acetate in hexane) gave 11.23 g (75.6%) of product as an oil, dried at 60° C. for 2 hours.

出典