HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 262217Generated: October 26, 2026
Diethyl Ether → 5-(alpha-Hydroxyundecyl)-3-phenylbenzofuran
https://huagongshe.com/reaction/262217
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 5-Bromo-3-phenyl-1-benzofuran | HCID 20330164 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(alpha-Hydroxyundecyl)-3-phenylbenzofuran | HCID 21320298 | — |
Reaction Steps
To a solution of 5.5 g. (0.02 mole) of 5-bromo-3-phenylbenzofuran in tetrahydrofuran is added 0.5 g. (0.02 mole) of magnesium, and the mixture is heated at its reflux temperature for three hours. After cooling to 0° C., 3.4 g. of undecyl aldehyde is added. After stirring for 30 minutes at room temperature, the solution is added to ammonium chloride solution. Evaporation provides a residue which is mixed with diethyl ether and water. The ether layer is separated, washed with saturated sodium chloride solution, dried and evaporated. The resulting oil is dissolved in carbon tetrachloride and eluted from a silica gel column with carbon tetrachloride, then with dichloromethane. The later fractions are evaporated to provide 5-(α-hydroxyundecyl)-3-phenylbenzofuran which is dissolved in dichloromethane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04153716 |
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| Source dataset | uspto-grants-1979_05 |
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| ORD ID | ord-c49d250a9e154af5b535095b9dcf3100 |
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| Source note | uspto-grants-1979_05 |
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