反応 #414345

反応方程式

water

thionyl chloride

3,3,3-trifluoro-2-hydroxy-2-methylpropanoic acid

4-(Phenylsulfonyl)benzenamine

→

N-[4-(Phenylsulfonyl)phenyl]-3,3,3,-trifluoro-2-hydroxy-2-methylpropanamide

溶媒

N,N-dimethylacetamide

反応条件

後処理

1. 1
   その他the mixture (a precipitate formed after a few minutes)
2. 2
   workup.STIRRINGto stir at room temperature overnight
3. 3
   ろ過the resulting solid was filtered off
4. 4
   洗浄washed with 3N HCl
5. 5
   乾燥water and dried at 65° C. for 2 hours
6. 6
   workup.DISSOLUTIONThe solid was dissolved in 300 mL of refluxing methylene chloride
7. 7
   workup.STIRRINGstirred
8. 8
   温度heated as hexane
9. 9
   workup.ADDITIONwas added
10. 10
    workup.ADDITIONWhen 250 mL of hexane had been added
11. 11
    その他(precipitate formed at about 180 mL addition) the mixture
12. 12
    濃縮was concentrated to 250 mL

実験手順

To a stirred, cooled (-20° C.) solution of 3,3,3-trifluoro-2-hydroxy-2-methylpropanoic acid (3.96 g 25 mmol) in N,N-dimethylacetamide (36 mL) was rapidly added thionyl chloride (3.10 g, 26 mmol) and the mixture (a precipitate formed after a few minutes) stirred at -15° C. to -5° C. for 1 hour. 4-(Phenylsulfonyl)benzenamine (3.97 g, 17 mmol) was then added in one portion and the mixture allowed to stir at room temperature overnight. The solution was poured into water, the resulting solid was filtered off, washed with 3N HCl, then water and dried at 65° C. for 2 hours. The solid was dissolved in 300 mL of refluxing methylene chloride and stirred and heated as hexane was added to replace the methylene chloride as it boiled off. When 250 mL of hexane had been added (precipitate formed at about 180 mL addition) the mixture was concentrated to 250 mL and refrigerated. The yield of light tan solid was 5.92 g (93%), mp 164°-166° C. 1H--NMR (250 MHz, d6 --DMSO): 1.59 (s, 3H, CH3), 7.57-7.72 (m, 4H, OH, aromatic), 7.92-8.04 (m, 6H, aromatic), 10.43 (s, 1H, NH).

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