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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282891Generated: October 30, 2026

Acetic Acid → 10,11-dihydro-10,10,11,11-tetrafluoro-5H-dibenzo[a,d]cyclohepten-5-one

https://huagongshe.com/reaction/1282891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrochloric AcidHCID 313—
Reactant10,11-dihydro-5,5,10,10,11,11-hexafluoro-5H-dibenzo[a,d]cyclohepteneHCID 20373324—
Product10,11-dihydro-10,10,11,11-tetrafluoro-5H-dibenzo[a,d]cyclohepten-5-oneHCID 20373376—

Reaction Conditions

Temperature65 °C

Reaction Steps

A solution of 989 mg. (0.00328 mole) of 10,11-dihydro-5,5,10,10,11,11-hexafluoro-5H-dibenzo[a,d]cycloheptene in 13.2 ml. of glacial acetic acid - 3.5 ml. of 6 N hydrochloric acid is held at room temperature for approximately 20 hours, heated in a 65°C. bath for 3 hours, again held at room temperature for about 20 hours, and finally heated in a 65°C. bath for 3 hours. The solution is concentrated under reduced pressure and the residue partitioned between benzene and water. The benzene extract is washed with water, dried over anhydrous sodium sulfate, and evaporated to dryness under reduced pressure. Sublimation of the residue at 80°C. and 0.1 mm. yields the crude product as an oily solid. Purification is effected by column chromatography on silica gel, the product being eluted with carbon tetrachloride. The fractions that show one spot of Rf 0.1 on a silica thin layer plate developed with carbon tetrachloride are combined. Evaporation of the solvent under reduced pressure leaves the white crystalline product, m.p. 76°-78°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03972936
Source datasetuspto-grants-1976_08
ORD IDord-7819b55861514a87b791f02abac3f958
Source noteuspto-grants-1976_08