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HRID 1583888作成日:2026年10月25日

1,2-Hexadecanediol → Pentadecanediol Octadecanediol

https://huagongshe.com/reaction/1583888

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-HexadecanediolHCID 98037—
反応物Pentadecane-1,2-diolHCID 118123—
反応物1,2-HeptadecanediolHCID 3015706—
反応物OctadecanediolHCID 20562952—
反応物DimethylphosphiteHCID 21884954—
溶媒MethanolHCID 887—
生成物Pentadecanediol OctadecanediolHCID 86740139—

反応条件

温度70 °C

反応手順

Approximately 360 g of 1,2-mixed pentadecanediol to octadecanediol (commercially obtained as Vikol 158 from Viking Chemical Co. and containing about 28% 1,2-pentadecanediol, about 28% 1,2-hexadecanediol, about 28% 1,2-heptadecanediol and about 16% octadecanediol, all percentages by weight) are charged to a glass reactor equipped with heater, agitator, Dean-Stark tube with condenser and provision for blanketing the vapor space with nitrogen. The contents were heated to 70° C. to liquify the solids and 55 g of dimethyl phosphite were slowly added. The reaction mixture was heated to 110° C. and held for 2 hours, held at 120° C. for 1 hour and held at 130° C. for 1 hour. Methanol was observed forming and collecting in the trap. The crude product was vacuum stripped at 150° C. to remove volatile materials, producing 375 g of intermediate additive. The intermediate was an amber fluid which became waxy after cooling.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04555353
出典データセットuspto-grants-1985_11
ORD IDord-1e15ba772b424052b21729cd74744121
出典メモuspto-grants-1985_11