反应 #1687648

反应方程式

acetyl chloride

pyridine

THF

sodium hydrogen carbonate

3,4-dihydro-6-hydroxy-2,5,7,8-tetramethyl-1-benzopyran-2-carboxylate

→

3,4-dihydro-6-acetyl-2,5,7,8-tetramethyl-1-benzopyran-2-carbonyl chloride

溶剂

water

反应条件

后处理

1. 1
   其他was reduced to 0° C.
2. 2
   温度refluxed for 1 hour
3. 3
   温度The solution was cooled
4. 4
   萃取The solution was extracted three times with DCM
5. 5
   干燥the DCM dried (sodium sulphate)
6. 6
   其他evaporated to dryness
7. 7
   workup.DISSOLUTIONThe hydroxy acetyl was redissolved in dry THF (100 ml)
8. 8
   workup.ADDITIONoxalyl chloride (10% solution 50 ml, excess) was slowly added at 10° C. under an atmosphere of di-nitrogen
9. 9
   温度to warm to ambient temperature
10. 10
    其他The clear solution was evaporated to dryness at 50° C.

实验过程

To a 1 liter round bottom flask with an atmosphere of di-nitrogen was added dry pyridine (10.00 g, excess mole) and dry THF solvent to dissolve 3,4-dihydro-6-hydroxy-2,5,7,8-tetramethyl-1-benzopyran-2-carboxylate (24.9 g). The temperature was reduced to 0° C. and acetyl chloride (15 ml) slowly added with agitation. The solution was observed to be yellow. The solution was allowed to warm up to ambient temperature and then refluxed for 1 hour. The solution was cooled, reduced in volume (100 ml) and water added with a sodium hydrogen carbonate (1 g). The solution was extracted three times with DCM, the DCM dried (sodium sulphate) and evaporated to dryness. The hydroxy acetyl was redissolved in dry THF (100 ml) and oxalyl chloride (10% solution 50 ml, excess) was slowly added at 10° C. under an atmosphere of di-nitrogen. The solution was allowed to warm to ambient temperature and stirred for 12 hours. The clear solution was evaporated to dryness at 50° C. and 10 mbar to give 3,4-dihydro-6-acetyl-2,5,7,8-tetramethyl-1-benzopyran-2-carbonyl chloride. The solid was washed with saturated sodium bicarbonate and vacuum dried. A carbon 13 NMR clearly showed the aromatic ring and the acetyl functionality.

来源