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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095250Generated: November 1, 2026

Formic Acid → HCID 58212295, compound

https://huagongshe.com/reaction/1095250

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantWaterHCID 962—
ReactantHCID 66781621HCID 66781621—
SolventTolueneHCID 1140—
ProductHCID 58212295HCID 5821229526.5%

Reaction Steps

The compound (25) (31.4 g), formic acid (90 g) and toluene (90 ml) were put in a reaction vessel under a nitrogen atmosphere, heated under reflux for 3 hours, and cooled slowly to room temperature. Water (200 ml) and toluene (200 ml) were added and mixed thereto. The mixture was allowed to stand until it had separated into two phases, the organic and aqueous phases, and an extractive operation to an organic phase was carried out. The organic phase was fractionated, and washed sequentially with a saturated aqueous solution of sodium hydrogencarbonate and water, and then dried over anhydrous magnesium sulfate. The solution was concentrated under reduced pressure, and the residue was purified with a fractional operation by means of column chromatography using a mixed solvent of toluene and ethyl acetate (toluene:ethyl acetate=9:1 by volume) as an eluent and silica gel as a stationary phase powder, and further purified by means of recrystallization from a mixed solvent of toluene and heptane (toluene: heptane=1:1 by volume), and dried, giving 7.51 g of 4′-(4-(4-ethoxycyclohexyl)-2-fluorophenyl)bi(cyclohexane)-4-one (26). The yield based on the compound (25) was 26.6%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08137583B2
Source datasetuspto-grants-2012_03
ORD IDord-110d0733bdbf42da9822ceeb976cff9c
Source noteuspto-grants-2012_03