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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 414168Erstellt: 26. Oktober 2026

Benzoic Acid → Icosan-9-yl benzoate

https://huagongshe.com/reaction/414168

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoic AcidHCID 243—
EduktHydrogen PeroxideHCID 784—
EduktSodium ChlorideHCID 5234—
EduktSodium CarbonateHCID 10340—
EduktPotassium HydroxideHCID 14797—
Edukt2-OctyldodecanolHCID 21414—
EduktSodium borohydrideHCID 4311764—
LösungsmittelWaterHCID 962—
ProduktIcosan-9-yl benzoateHCID 53719708—

Reaktionsbedingungen

Temperatur255 °C

Reaktionsschritte

A mixture of 213 gms. (0.715 moles) of STANDAMUL G from Henkel Co. (Octyldodecanol) and 15 mgms. Sodium borohydride was stirred at room temperature 25° C. under nitrogen. The mixture was then heated and brought to 60° C. and held at 60° C. for 1/2 hour. To this mixture was added 86.40 gms. (0.68 moles) Benzoic Acid and 450 mgms. of stannous oxalate. The reaction mixture was then further heated to 255° C. During the heat-up cycle, distillate was collected, particularly when the reaction mixture reached a temperature of 170° C. and higher. The reaction was rapidly heated from 60° C. to 177° C. over 45 minutes, and then from 177° C. to 228° C. over the next 60 minutes while still collecting the distillate. Further heating was continued to bring the temperature to 255° C. over the next 30 minutes. The distillate collected contained 7.5 gms. of water and also contained some benzoic acid trapped during the collection of distillate. The reaction was then cooled. The yield at this stage was 265 gm. and acidity was at 9.5 mgms. The KOH/gm. hydroxyl value of this mixture was 19.29. 220 gms. of this ester was treated with 2.2 gms. sodium carbonate, 1.1 gm. sodium chloride, 2.0 gms. Hydrogen peroxide in 35 gms. deionized water. The mixture was stirred and heated to 85°-90° C., held at 85°-90° C. for 30 minutes and allowed to stand for separation of the ester and water phases. The ester phase was separated and further washed with deionized water until reaction of the water was neutral. The ester collected was 200 gms. and was hydrous. The product was vacuum stripped to remove the residual moisture, and then filtered using filter-aids. The final product was a clear liquid and had the following formula: ##STR11##

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04791097
Quelldatensatzuspto-grants-1988_12
ORD IDord-9cbd83e3b0134812b8d34877703098a7
Quellennotizuspto-grants-1988_12