HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050443Generated: November 1, 2026
4-Fluorobenzoyl chloride → HCID 178525712, compound
https://huagongshe.com/reaction/2050443
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Fluorobenzoyl chloride | HCID 67879 | — |
| Reactant | HCID 178521563 | HCID 178521563 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 178525712 | HCID 178525712 | — |
Reaction Steps
A solution of 1.7 g of 4-fluorobenzoyl chloride in 5 ml of pyridine is treated with 2.8 g of trans-4-[trans-4-[2-(1,3-dioxolan-2-yl)ethyl]cyclohexyl]cyclohexanol (prepared according to Example 1) and stirred at room temperature for 12 hours. Thereafter, the reaction mixture is poured on to ice-water and extracted three times with diethyl ether. The organic phases are washed in succession with saturated sodium hydrogen carbonate solution, with 10 percent hydrochloric acid, with saturated sodium hydrogen carbonate solution and with water, then dried over magnesium sulfate, filtered and concentrated. Chromatographic purification of the resulting crude product on silica gel with ethyl acetate/petroleum ether (vol. 3:97) gives 4-fluorobenzoic acid trans-4-[trans-4-[2-(1,3-dioxolan-2-yl)ethyl]cyclohexyl]cyclohexyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05013477 |
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| Source dataset | uspto-grants-1991_05 |
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| ORD ID | ord-36e59ce4246c4e6b862eaa901af70843 |
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| Source note | uspto-grants-1991_05 |
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