HRID359939

反应详情

EQUATION

反应方程式

HRID 359939 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A 12-L three-neck, round-bottom flask equipped with a mechanical stirrer and a nitrogen bubbler, was charged with 375.0 g (1.79 moles) of 5-bromo-1-pentanyl acetate, 3.5 L of dimethyl sulfoxide, 407.0g (1.63 moles) of rac-6-acetyl-3, 4-dihydro-7-hydroxy-2H-1-benzopyran-2-carboxylic acid methyl ester and 510.0 g of anhydrous granular potassium carbonate in finely powdered form. The mixture was stirred at room temperature under nitrogen for 19 hours, poured into an extractor containing 10 L of deionized water, and extracted with 2×4 L and 1×2 L=10 L of ethyl acetate. The organic layer was washed with 2×4 L=8 L of 1:1 deionized water-saturated brine, followed by 2 L of saturated brine, dried (anhydrous sodium sulfate), and filtered. The solvent was removed at 45° /70 mm and then under high vacuum to give 648.3 g of crude rac-6-acetyl-3,4-dihydro- 7-[(5-acetoxypentyl)oxy]-2H-1-benzopyran-2-carboxylic acid methyl ester. The crude product was dissolved in 2 L of anhydrous ether and the solution was poured into a 12 L three-neck flask equipped with a mechanical stirrer. The stirred solution was cooled in an ice-bath and 2 L of petroleum ether (35°-60° ) was slowly added, which resulted in the formation of a precipitate heavy enough to stop the stirrer. The solid was broken with a spatula and stirring was continued in the ice-bath for 1 hour. The product was collected by filtration, washed with cold (3° ) 1:1 ether-petroleum ether, and dried at room temperature under high vacuum to give 601.5 g (97.7& yield) of rac-6-acetyl-3,4-dihydro-7-[(5-acetoxypentyl)oxy]-2H-1-benzopyran-2-carboxylic acid methyl ester as a white powder, mp 37°-49° C. UV (EtOH): λmax, 312 (ε=7,200), 268 (ε=11,200), 230 (ε=16,900), and 216 (ε=19,000) nm; MS: m/z 378 (M+, 40).

WORKUP

后处理

  1. customA 12-L three-neck, round-bottom flask equipped with a mechanical stirrer
  2. additionpoured into an extractor
  3. extractionextracted with 2×4 L and 1×2 L=10 L of ethyl acetate
  4. washThe organic layer was washed with 2×4 L=8 L of 1:1 deionized water-saturated brine
  5. dry with materialdried (anhydrous sodium sulfate)
  6. filtrationfiltered
  7. customThe solvent was removed at 45° /70 mm