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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727983Generated: October 30, 2026

HCID 19824462, compound → HCID 19824463, compound

https://huagongshe.com/reaction/727983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 19824462HCID 19824462—
CatalystPalladiumHCID 23938—
ProductHCID 19824463HCID 19824463—

Reaction Steps

By customary procedures, 3.5 g of benzyl 4-undecylcarboxybenzoate was prepared from 2.3 g of benzyl 4-hydroxybenzoate and 2.5 g of lauric acid chloride, and this ester was catalytically reduced under a hydrogen pressure of 2 kg/cm2 by using Pd/C as the catalyst to obtain 2.8 g of 4-undecylcarboxybenzoic acid. The acid was converted to 4-undecylcarboxybenzoic acid chloride by thionyl chloride and the acid chloride was reacted with 1.8 g of benzyl 4-hydroxybenzoate to form benzyl 4-(4-undecylcarboxybenzoyloxy)benzoate. The ester was catalytically reduced under a hydrogen pressure of 2 kg/cm2 by using Pd/C as the catalyst to isolate the benzyl group and obtain 3.0 g of 4-(4'undecylcarboxybenzoyloxy)benzoic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05045228
Source datasetuspto-grants-1991_09
ORD IDord-4324c6caccff4871989da802cf527d71
Source noteuspto-grants-1991_09