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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2309669Generated: November 2, 2026

3,4-Difluorobenzoyl chloride → HCID 178444574, compound

https://huagongshe.com/reaction/2309669

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Difluorobenzoyl chlorideHCID 2724519—
ReactantHCID 178444573HCID 178444573—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
SolventTolueneHCID 1140—
ProductHCID 178444574HCID 17844457470%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of trans-4-pentylcyclohexanol (1.9 g 0.011 mol) dissolved in dry pyridine (5 ml) was added a solution of 3,4-difluorobenzoyl chloride (2.0 g, 0.011 mol) dissolved in dry toluene (10 ml), followed by heating the mixture at 60° C. for 3 hours, thereafter pouring the reaction mixture in water (100 ml), separating the toluene layer, washing it with 6N hydrochloric acid, then with 2N-NaOH aqueous solution and further with water, drying with anhydrous sodium sulfate, distilling off toluene from the resulting toluene solution and recrystallizing the remaining oily product from ethanol to obtain the objective 3,4-difluorobenzoic acid-trans-4-pentylcyclohexyl ester (2.4 g, 0.0077 mol) (yield: 70%). This product has a m.p. of 26.9° C., and its N-I point sought from a mixture thereof with trans-4-alkyl-(4-cyanophenyl)cyclohexanes according to extrapolation method was -6.0° C. Further its elemental analysis values were as follows: C: 70.03%, H: 7.81% (calculated values, C: 69.65% and H: 7.79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04696759
Source datasetuspto-grants-1987_09
ORD IDord-baaa3c427b084013b72c2aed22a11d74
Source noteuspto-grants-1987_09