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HRID 371370作成日:2026年10月27日

1,2-Octadecanediol → Pentadecanediol Octadecanediol

https://huagongshe.com/reaction/371370

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-OctadecanediolHCID 89314—
反応物Dimethyl ester phosphorous acidHCID 94853—
反応物1,2-HexadecanediolHCID 98037—
反応物Pentadecane-1,2-diolHCID 118123—
反応物1,2-HeptadecanediolHCID 3015706—
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 the 1,2-mixed pentadecanedioloctadecanediol (obtained from Viking Chemical Co. as Vikol 158 containing about 28% 1,2-pentadecanediol, about 28% 1,2-hexadecanediol, about 28% 1,2-heptadecanediol and about 16% 1,2-octadecanediol) were 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 and 55 g of dimethyl hydrogen 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. During this reaction period, methanol distilled over and condensed into the trap. The crude product was vacuum stripped at 150° C. to remove volatile materials. 379 g of finished additive were produced. The product was an amber fluid which became waxy on cooling.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04532057
出典データセットuspto-grants-1985_07
ORD IDord-edebad08f5b148ccac7479e949a5f540
出典メモuspto-grants-1985_07