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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1886721Generated: November 1, 2026

Formic Acid → 4'-(4-Butoxy-2,3-difluorophenyl)-bicyclohexyl-4-one

https://huagongshe.com/reaction/1886721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantWaterHCID 962—
Reactant8-[4-(4-Butoxy-2,3-difluorophenyl)-cyclohexenyl]-1,4-dioxaspiro[4.5]decaneHCID 66680923—
SolventTolueneHCID 1140—
Product4'-(4-Butoxy-2,3-difluorophenyl)-bicyclohexyl-4-oneHCID 6668377598.5%

Reaction Conditions

Temperature30 °C

Reaction Steps

The compound (23) (7.7 g), formic acid (87%; 8.7 g) and toluene (100 ml) were mixed and the mixture was heated to reflux for 2 hours. After the reaction mixture had been cooled to 30° C., water (200 ml) and toluene (200 ml) were added to the mixture and mixed with it. The mixture was then allowed to stand until it had separated into two phases of organic and aqueous phases, and the extraction into an organic phase was carried out. The resulting organic phase was separated, and washed successively with water, a saturated aqueous solution of sodium hydrogencarbonate and water, and then dried over anhydrous magnesium sulfate. Then the solvent was distilled off under reduced pressure, and the residue was purified by recrystallization from heptane solvent and dried to give 4′-(4-butoxy-2,3-difluorophenyl)-bicyclohexyl-4-one (24) (6.8 g). The yield based on the compound (23) was 99.0%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501038B2
Source datasetuspto-grants-2013_08
ORD IDord-f71525002d68406798f03c48152d9988
Source noteuspto-grants-2013_08