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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371370Generated: October 25, 2026

1,2-Octadecanediol → Pentadecanediol Octadecanediol

https://huagongshe.com/reaction/371370

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-OctadecanediolHCID 89314—
ReactantDimethyl ester phosphorous acidHCID 94853—
Reactant1,2-HexadecanediolHCID 98037—
ReactantPentadecane-1,2-diolHCID 118123—
Reactant1,2-HeptadecanediolHCID 3015706—
SolventMethanolHCID 887—
ProductPentadecanediol OctadecanediolHCID 86740139—

Reaction Conditions

Temperature70 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04532057
Source datasetuspto-grants-1985_07
ORD IDord-edebad08f5b148ccac7479e949a5f540
Source noteuspto-grants-1985_07