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HRID 1651015作成日:2026年10月27日

Tetraethylenepentamine → Dihydroxypropyl carbamate

https://huagongshe.com/reaction/1651015

反応式

関与物質

役割名称HCID仕込み量
反応物TetraethylenepentamineHCID 8197—
反応物Sodium HydroxideHCID 14798—
反応物(2-Methyl-2-propenyl)succinic AnhydrideHCID 225375—
反応物CarbonochloridateHCID 21226386—
反応物Glycerol di(trichloroacetate)HCID 23050921—
溶媒TolueneHCID 1140—
溶媒HexaneHCID 8058—
生成物Dihydroxypropyl carbamateHCID 57197969—

反応条件

温度-2 °C

反応手順

The chloroformate of glycerol di(trichloroacetate), 42.3 g, is dissolved in 200 ml toluene. 300 Grams of a monosuccinimide dispersant composition (prepared by reacting 1 mole of polyisobutenyl succinic anhydride, where the polyisobutenyl group has a number average molecular weight of about 950, with 0.87 mole of tetraethylene pentaamine then diluting to about 50% actives in diluent oil) is dissolved in 200 ml toluene. Both solutions are cooled to below 0° C. (approximately -2° C.) using a salt ice-water bath. The solutions are poured together into a 2-liter flask equipped with a mechanical stirrer and a drying tube. The reaction solution is mixed with strong stirring and kept below 0° C. for 40 minutes and then is allowed to warm to room temperature. After stirring at room temperature for several hours, about 65 mls of the reaction mixture is added to 130 mls hexane and 65 mls 1N NaOH in a separatory funnel in order to remove the trichloroacetate group. The mixture is intermittently shaked for 30 minutes. After phase separation, the organic layer is washed several times with brine, is dried over anhydrous magnesium sulfate, is filtered and stripped to yield dihydroxypropyl carbamate derivatives of the monosuccinimide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04927551
出典データセットuspto-grants-1990_05
ORD IDord-8e17d1df15bd481a9897096c8c49e220
出典メモuspto-grants-1990_05