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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033230Generated: October 26, 2026

3,3,5-Trimethylcyclohexanol → HCID 86747828, compound

https://huagongshe.com/reaction/1033230

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,3,5-TrimethylcyclohexanolHCID 8298—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2-DimethylaminopyridineHCID 21885—
ReactantBezafibrateHCID 39042—
SolventDimethylformamideHCID 6228—
ProductHCID 86747828HCID 8674782845%

Reaction Steps

12.5 g (0.034 mol) of 2-(4-(2-parachlorobenzamidoethyl)phenoxy)-2-methylpropionic acid are dissolved in 100 ml of anhydrous dimethylformamide, and 4.8 g of 3,3,5-trimethylcyclohexanol (transform) (0.034 mol) and 0.5 g of dimethylaminopyridine are added. After solubilization, a solution of 7 g of dicyclohexylcarbodiimide (0.034 mol) in 20 ml of dimethylformamide is added slowly at a temperature of around 0° C. The reaction is allowed to continue for 24 hours at ordinary temperature and the precipitate of dicyclohexylurea is filtered off; after evaporation of the filtrate under reduced pressure, the residue is chromatographed on a silica column in a mixture of petroleum ether and ethyl acetate. After evaporation of the solvent, the title derivative is obtained in the form of white crystals melting at 100° C.; the yield is 45%. This product, chromatographed under the conditions of Example 1, shows a single spot of Rf 0.2. The IR spectrum run in KBr has the following characteristic bands: one broad band at 3250 cm-1, a group of fine bands at 3000-2840 cm-1 an strong bands at 1750 cm-1 and 1640 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05310757
Source datasetuspto-grants-1994_05
ORD IDord-ae14080d5f44417ab20d4b46b2520081
Source noteuspto-grants-1994_05