HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1102Generated: October 23, 2026
1-Tetradecanol → 1,2-Epoxy-2-methyl-3-tetradecyloxypropane
https://huagongshe.com/en/reaction/1102
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Tetradecanol | HCID 8209 | — |
| Reactant | 3-Chloro-2-methyl-1-propene | HCID 11241 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1,2-Epoxy-2-methyl-3-tetradecyloxypropane | HCID 19694608 | 79.5% |
Reaction Steps
A 200-ml flask equipped with a stirrer was charged with 10 g (46.6 mmol) of tetradecanol, 50 ml of dimethylformamide, 2.86 g (71.5 mmol) of 60% NaH and 5.96 g (65.8 mmol) of methallyl chloride. The contents were stirred at 60° C. for 15 hours. After completion of the reaction, the reaction mixture was added with water and subjected to extraction with hexane, and the solvent was distilled off under reduced pressure. The resultant residue was charged into a 300-ml flask equipped with a stirrer, and 12.24 g (70.9 mmol) of m-chloroperbenzoic acid and 200 ml of dichloromethane were added thereto. The resultant mixture was stirred at room temperature for 19 hours. Solids formed were separated by filtration, and the resultant solution was concentrated under reduced pressure and then purified by column chromatography on silica gel, thereby obtaining 10.54 g (yield: 79.4%) of 1,2-epoxy-2-methyl-3-tetradecyloxypropane as an intermediate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05723497 |
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| Source dataset | uspto-grants-1998_03 |
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| ORD ID | ord-cb6871243aa046c0acd17a0fc444cdcb |
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| Source note | uspto-grants-1998_03 |
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