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HRID 326894作成日:2026年10月25日

Isopropanol → 4,4-Dihydroxy-alpha-methylstilbene

https://huagongshe.com/reaction/326894

反応式

関与物質

役割名称HCID仕込み量
反応物IsopropanolHCID 3776—
反応物EpichlorohydrinHCID 7835—
反応物Sodium HydroxideHCID 14798—
反応物4,4'-Dihydroxy-alpha-methylstilbeneHCID 656693—
溶媒WaterHCID 962—
生成物4,4-Dihydroxy-alpha-methylstilbeneHCID 69933604—

反応条件

温度55 °C

反応手順

4,4'-Dihydroxy-alpha-methylstilbene 152.73 grams, 1.35 hydroxyl equivalents) from A above, epichlorohydrin (624.58 grams, 6.75 moles), deionized water (54.31 grams, 8.0 percent by weight of the epichlorohyrin used) and isopropanol (336.31 grams, 35 percent by weight of the epichlorohydrin used) is added to a reactor and heated to 55° C. with stirring under a nitrogen atmosphere. Once the 55° C. reaction temperature is achieved, sodium hydroxide (48.6 grams, 1.22 moles) dissolves in deionized water (194.4 grams) is added dropwise to the reactor over a 45 minute period so as to maintain reaction temperature between 55° and 59° C. Ten minutes after completion of the aqueous sodium hydroxide addition, the stirring is stopped and the aqueous layer which separated from the reaction mixture is pipetted off and discarded. Stirring is resumed and after a total of twenty minutes following completion of the initial aqueous sodium hydroxide addition, a second solution of sodium hydroxide (21.6 grams, 0.54 mole) dissolved in deionized water (86.4 grams) is added to the reactor over a twenty minute period 30 as to maintain the 55° C. reaction temperature. Fifteen minutes after completion of the aqueous sodium hydroxide addition, the recovered reaction mixture is added to a separatory funnel and washed with 750 milliliters of deionized water. The separated organic layer is washed a second time (750 milliliters deionized water), recovered and then rotary evaporated under vacuum for 45 minutes at 110° C. then 30 minutes at 130° C. The product is recovered (218.6 grams) as a crystalline solid with an epoxide equivalent weight of 183.33.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05270405
出典データセットuspto-grants-1993_12
ORD IDord-9824c80c642b4f3da2f21b708132930f
出典メモuspto-grants-1993_12