反応 #464376

反応方程式

Magnesium

iodine crystals

bromide

magnesium

Phenylpropylmagnesium bromide

Diethylchlorophosphite

Phenylpropyl bromide

→

3-phenylpropylphosphinic acid

収率 53.2%

溶媒

diethyl ether

water

diethyl ether

diethyl ether

反応条件

後処理

1. 1
   その他After several minutes the iodine was consumed
2. 2
   workup.ADDITIONadditional phenylpropyl bromide was added
3. 3
   その他(1.5 hours)
4. 4
   その他was sealed
5. 5
   その他stored at 5° C
6. 6
   温度while maintaining a temperature between 0-10° C
7. 7
   その他A thick white slurry formed
8. 8
   workup.STIRRINGwas stirred an additional 30 minutes
9. 9
   ろ過The mixture was filtered under a nitrogen atmosphere
10. 10
    その他the filtrate evaporated under reduced pressure
11. 11
    その他to give a clear and colorless liquid
12. 12
    その他An exothermic reaction
13. 13
    workup.STIRRINGstirring
14. 14
    抽出followed by extraction with ethyl acetate
15. 15
    洗浄washed with brine
16. 16
    乾燥dried (MgSO4)
17. 17
    その他evaporated
18. 18
    workup.ADDITIONTo the clear liquid was added sodium hydroxide (40 mL, 2.0 M NaOH)
19. 19
    workup.STIRRINGthe resulting solution stirred for 1 hour
20. 20
    洗浄washed with diethyl ether
21. 21
    抽出extracted twice with ethyl acetate
22. 22
    乾燥dried (MgSO4)
23. 23
    その他evaporated

実験手順

Magnesium turnings (2.44 g, 0.10 mol) in 20 mL of dry diethyl ether under an atmosphere of nitrogen was added several iodine crystals. Phenylpropyl bromide (20.0 g, 0.10 mol) in 80 mL of diethyl ether was placed in a dropping funnel. Approximately 10 mL of the bromide solution was added to the magnesium turnings and stirring was initiated. After several minutes the iodine was consumed and additional phenylpropyl bromide was added while maintaining a temperature of 35° C. Once additional was complete (1.5 hours) the mixture was sealed and stored at 5° C. Diethylchlorophosphite (15.7 g, 0.1 mol) in 50 mL of dry diethyl ether was cooled to 5° C. under an atmosphere of nitrogen. Phenylpropylmagnesium bromide (100 mL, 0.1 mol, 1.0 M solution of in Et2O) was added dropwise over 2 hours while maintaining a temperature between 0-10° C. A thick white slurry formed and was stirred an additional 30 minutes. The mixture was filtered under a nitrogen atmosphere and the filtrate evaporated under reduced pressure to give a clear and colorless liquid. To the liquid was added 20 mL of water followed by 0.5 ml of concentrated hydrlochloric acid. An exothermic reaction was observed and stirring continued for 20 minutes followed by extraction with ethyl acetate. The organics were combined, washed with brine, dried (MgSO4) and evaporated. To the clear liquid was added sodium hydroxide (40 mL, 2.0 M NaOH), the resulting solution stirred for 1 hour and then washed with diethyl ether. The aqueous layer was acidified to pH 1.0 with concentrated hydrochloric acid and extracted twice with ethyl acetate. The organics were combined, dried (MgSO4) and evaporated to give 3-phenylpropylphosphinic acid (1,R=CH2CH2CH2Ph,R1=H)(9.8 g, 53%) as a clear and colorless oil.

出典