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HRID 482942作成日:2026年10月26日

Isopropyl Isostearate → Isostearyl Alcohol EX

https://huagongshe.com/reaction/482942

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

Into a 20 liters autoclave were charged 4770 g of isopropyl isostearate [Emery 2310, commercially available from Emery Co., Ltd. U.S.A.] and 239 g of copper-chromium catalyst (product of Nikki Co., Ltd.). Hydrogen gas was charged into the reactor under a pressure of 150 kg/cm2 and the reaction mixture was heated up to 275° C. After hydrogenation under 150 kg/cm2 /275° C. for about 7 hours, the reaction product was cooled, followed by removing the catalyst residue by filtration to obtain 3500 g of crude product. The crude product was distilled under reduced pressure thereby obtaining 3300 g of colorless transparent isostearyl alcohol as a fraction of 80° to 167° C./0.6 mmHg. The thus obtained isostearyl alcohol (monomethyl-branched isostearyl alcohol) had an acid value of 0.05, a saponification value of 5.5, and a hydroxyl value of 181.4. IR analysis (liquid film) revealed absorptions at 3340 and 1055 cm-1 and NMR analysis (CCl4 solvent) revealed an absorption at (δ)=3.50 (broad triplet, --CH2 --OH). According to the gas chromatograph, the alcohol was chiefly composed of about 75% of an alcohol whose number of carbon atoms in the alkyl group was 18, with the remainder being made of alcohols having alkyl groups with 14 and 16 carbon atoms. The branched methyl group was located substantially at the center of the main alkyl chain in all the alcohol components.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04576967
出典データセットuspto-grants-1986_03
ORD IDord-dc66600bfb2e47ad95e3fd2e2b86c686
出典メモuspto-grants-1986_03