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HRID 979881作成日:2026年10月25日

Isopropyl Isostearate → Isostearyl Alcohol EX

https://huagongshe.com/reaction/979881

反応式

関与物質

役割名称HCID仕込み量
反応物Isopropyl IsostearateHCID 94625—
反応物HCID 178418361HCID 178418361—
触媒Chromium, compd. with copper (1:1)HCID 9833946—
生成物Isostearyl Alcohol EXHCID 6282583.5%

反応条件

温度275 °C

反応手順

4770 g of isostearic acid isopropyl ester (Emery 2310 isostearic acid isopropyl ester, sold by Emery Industry Inc., U.S.A.) and 239 g of a copper-chromium catalyst (made by Nikki) are charged in an autoclave having a capacity of 20 liters. Hydrogen gas is then added under a pressure of 150 kg/cm2 and the reaction mixture is heated to a temperature of 275° C. Hydrogenation was carried out under a pressure of 150 kg/cm2 at 275° C. for about 7 hours, and then the reaction product was cooled and the catalyst residue was removed by filtration, whereupon 3500 g of a crude product were obtained. The crude product was distilled under reduced pressure thereby obtaining 3300 g of a colourless transparent isostearyl alcohol as a distillate at 80° to 167° C./0.6 mmHg. The isostearyl alcohol (methyl-branched stearyl alcohol) thus prepared had an acid value of 0.05, a saponification value of 5.5, and a hydroxyl value of 181.4. Absorption was observed at 3340 and 1055 cm-1 by IR (liquid film) and at δ3.50 (broad triplet, --CHH2 --OH) by NMR(CCl4). It has been found from gas-chromatography that the alcohol consists of a mixture which comprises about 75% of the main component having a total carbon number of 18 (the total of m and n being 15 in the formula II) and the rest being composed of components having a total carbon number of 14 or 16, and that, in any case, branched methyl groups are located in the vicinity of the center of the main alkyl chain.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04634719
出典データセットuspto-grants-1987_01
ORD IDord-ca70944ccc734fbe83ecdd385e909f4b
出典メモuspto-grants-1987_01