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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 83772생성일: 2026년 10월 24일

Oxygen → 3-Hydroxy-1-adamantyl acrylate

https://huagongshe.com/ko/reaction/83772

반응식

참여 물질

역할이름HCID투입량
반응물OxygenHCID 977—
반응물Sulfuric AcidHCID 1118—
반응물Acrylic AcidHCID 6581—
반응물4-MethoxyphenolHCID 9015—
반응물Sodium HydroxideHCID 14798—
반응물1,3-AdamantanediolHCID 573829—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물3-Hydroxy-1-adamantyl acrylateHCID 22228790—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846840B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-5b49aa7245f240439839520096704a9f
출처 메모uspto-grants-2014_09