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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 8-[4-(4-Butoxy-2,3-difluorophenyl)-cyclohexenyl]-1,4-dioxaspiro[4.5]decane | HCID 66680923 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4'-(4-Butoxy-2,3-difluorophenyl)-bicyclohexyl-4-one | HCID 66683775 | 98.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08501038B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-f71525002d68406798f03c48152d9988 |
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| Source note | uspto-grants-2013_08 |
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