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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1382032Generated: November 2, 2026

Lauric Acid → Lauric Acid

https://huagongshe.com/reaction/1382032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLauric AcidHCID 3893—
ReactantHCID 178418361HCID 178418361—
ProductLauric AcidHCID 3893—
Product1-DodecanolHCID 8193—

Reaction Conditions

Temperature60 °C

Reaction Steps

700 g of catalyst produced in accordance with formulation 3. above were introduced into a continuous recycle-gas pilot plant having a reactor volume of 1 liter and activated as described above. Thereafter, 100 ml/h of pure lauric acid, which had been preheated to 240° C., was passed over the catalyst in the presence of hydrogen recirculated at a rate of 16 l/h under a pressure of 250 bars (corresponding to 4 m3 /h in the absence of pressure; equal to a 178.5-fold molar excess) at 270° C. Most of the lauric acid evaporated on the catalyst. The hydrogen leaving the reactor was cooled to about 60° C., the hydrogenation product separating and being relieved of pressure. 1 kg of lauric acid produced 920 g of pure lauryl alcohol which accumulated in colorless form with a saponification number of 0.5, an acid number of 0.06, a paraffin content of 0.96% and a low water content. After drying, its hydroxyl number was 299. The aldehyde content of 215 ppm of CO was very low. After about 140 hours' operation under the described conditions, the saponification number rose to 5.2. Because of this, the reactor entry temperature (reaction temperature) was increased to 300° C., as a result of which the saponification number fell below 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04804790
Source datasetuspto-grants-1989_02
ORD IDord-5d3efe4c7ada4a55ad8b82cf06ce023b
Source noteuspto-grants-1989_02