HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330222Generated: October 30, 2026
Potassium Hydroxide → (S)-5-(8-methyldecyloxy)-2-(4-octyloxyphenyl)pyrimidine
https://huagongshe.com/reaction/330222
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-(4-(Octyloxy)phenyl)pyrimidin-5-ol | HCID 14496395 | — |
| Reactant | (S)-8-methyldecyl bromide | HCID 14496397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (S)-5-(8-methyldecyloxy)-2-(4-octyloxyphenyl)pyrimidine | HCID 14496399 | 29.7% |
Reaction Steps
KOH (0.8 g) was added to a solution of 5-hydroxy-2-(4-octyloxyphenyl)pyrimidine (4 g) dissolved in ethanol (20 ml), followed by adding (S)-8-methyldecyl bromide (3.2 g) prepared according to the method disclosed in the literature (Mol. Cryst. Liq. Cryst., 1984, Vol. 114, pp. 237-247), keeping the mixture under reflux for 6 hours, allowing the resulting material to cool down, extracting it with toluene, washing the resulting organic layer with 2N-NaOH aqueous solution, further washing with water until the washing water became neutral, distilling off low-boiling components in the organic layer and recrystallizing the residue from ethanol to obtain the captioned compound, (S)-5-(8-methyldecyloxy)-2-(4-octyloxyphenyl)pyrimidine (1.8 g). Its phase transition points were as follows: ##STR12##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04895671 |
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| Source dataset | uspto-grants-1990_01 |
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| ORD ID | ord-c6406eb115c34adbb01cf521c9a59aec |
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| Source note | uspto-grants-1990_01 |
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