Реакция #170954

Уравнение реакции

1,3-adamantanediol

p-methoxyphenol

sulfuric acid

sodium hydroxide

oxygen

p-methoxyphenol

acrylic acid

sulfuric acid

acrylic acid

→

3-hydroxy-1-adamantyl acrylate

Растворители

water

toluene

water

water

Условия реакции

Обработка

1. 1
   ДругоеTo a 2 L jacket-equipped separable flask
2. 2
   Другоеprovided with a stirrer
3. 3
   ДругоеPrepared gas
4. 4
   workup.ADDITIONdiluted with nitrogen so as
5. 5
   ТемператураWhile the solution was heated
6. 6
   Другоеwas removed by the Dean-Stark water separator
7. 7
   ДругоеThus, 3-hydroxy-1-adamantyl acrylate was synthesized
8. 8
   ДругоеThe obtained reaction solution
9. 9
   ПромывкаThe resultant solution was washed with 5% by weight of dilute sulfuric acid and with 500 ml of ion exchange water
10. 10
    ФильтрацияAfter the washing, precise filtration
11. 11
    Фильтрацияfilter
12. 12
    ТемператураThen, cooling
13. 13
    Другоеcrystallization
14. 14
    Другоеwas performed at a temperature of an ice water bath
15. 15
    Другоеto separate the crystal
16. 16
    Фильтрацияby filtration
17. 17
    ПромывкаThe crystal was rinsed with heptane twice
18. 18
    Другоеdried at a reduced pressure at 25° C. for 24 hours
19. 19
    ДругоеDuring the process from the dehydration esterification reaction
20. 20
    Другоеto the solid-liquid separation
21. 21
    Промывкаuntil the termination of rinsing

Методика

To a 2 L jacket-equipped separable flask provided with a stirrer, a thermometer, a Dean-Stark water separator, a Dimroth condenser and a prepared gas introduction tube, 84 g of 1,3-adamantanediol, 108 g of acrylic acid, 0.76 g of p-methoxyphenol as a polymerization inhibitor, 1.3 g of concentrated sulfuric acid as an acid catalyst, and 750 ml of toluene as a solvent were put. Prepared gas diluted with nitrogen so as to have an oxygen concentration of about 5% by volume was supplied at a rate of 0.2 L/min. The reaction operation was performed as follows. While the solution was heated and water generated as a secondary product was removed by the Dean-Stark water separator, the reflux state was continued for 6 hours. Thus, 3-hydroxy-1-adamantyl acrylate was synthesized. The obtained reaction solution was cooled down to room temperature, and then a 10% by weight of aqueous solution of sodium hydroxide was added while stirring to neutralize the residual acrylic acid and sulfuric acid. Then, the neutralized water phase was drawn out from the two-phase solution. To the residual organic phase, 0.85 g of p-methoxyphenol was added as a polymerization inhibitor. The resultant solution was washed with 5% by weight of dilute sulfuric acid and with 500 ml of ion exchange water, twice for each. After the washing, precise filtration was performed by use of a Teflon® filter having a pore diameter of 0.1 μm. Then, cooling crystallization was performed at a temperature of an ice water bath to separate the crystal by filtration. The crystal was rinsed with heptane twice, and then dried at a reduced pressure at 25° C. for 24 hours. During the process from the dehydration esterification reaction to the solid-liquid separation and until the termination of rinsing performed by use of ion exchange water, the prepared gas was kept blown into the solution. Table 1 shows the analysis results of the obtained 3-hydroxy-1-adamantyl acrylate. Methylethylketone was used as the solvent for measuring the turbidity.

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