HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486347Generated: October 28, 2026
Water → (+)-5-Octyl-2-[4-(2-fluoroheptyloxy)phenyl]pyrimidine
https://huagongshe.com/reaction/486347
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(4-Hydroxyphenyl)-5-octylpyrimidine | HCID 604055 | — |
| Reactant | (+)-2-Fluoroheptyl p-toluenesulfonate | HCID 14716844 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | (+)-5-Octyl-2-[4-(2-fluoroheptyloxy)phenyl]pyrimidine | HCID 14597237 | — |
Reaction Steps
0.43 g (1.5 mmol) of the thus obtained (+)-2-fluoroheptyl p-toluenesulfonate and 0.28 g (1.0 mmol) of 5-octyl-2-(4-hydroxyphenyl)pyrimidine were mixed with 0.2 ml of 1-butanol, followed by sufficient stirring. To the solution was quickly added a previously obtained alkaline solution of 0.048 g (1.2 mmol) of sodium hydroxide in 1.0 ml of 1-butanol, followed by 5.5 hours of heat-refluxing. After the reaction, 10 ml of distilled water was added, and the mixture was extracted respectively once with 10 ml of benzene and 5 ml of benzene, followed by drying with an appropriate amount of anhydrous sodium sulfate, distilling-off of the solvent and purification by silica gel column chromatography (chloroform) to obtain 0.17 g (0.43 mmol) of objective (+)-5-octyl-2-[4-(2-fluoroheptyloxy)phenyl]pyrimidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05292453 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-3d2093320e0146a1bf73a1075767c56c |
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| Source note | uspto-grants-1994_03 |
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