HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2014Generated: October 23, 2026
Sodium Chloride → Diethyl 1-methyl-5-(tetrahydropyran-2-yloxy)pentylphosphonate
https://huagongshe.com/en/reaction/2014
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Diethyl 5-(tetrahydropyran-2-yloxy)pentylphosphonate | HCID 19689209 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Diethyl 1-methyl-5-(tetrahydropyran-2-yloxy)pentylphosphonate | HCID 19689181 | — |
Reaction Steps
30 g (0.097 mol) of diethyl 5-(tetrahydropyran-2-yloxy)pentylphosphonate were initially introduced into 200 ml of absolute tetrahydrofuran under an argon atmosphere, cooled to -70° C. and treated with 42.8 ml (0.107 mol) of a 2.5 molar solution of butyllithium in hexane. After addition, the solution was stirred for a further 30 minutes and 15.6 g (0.11 mol) of methyl iodide were then slowly added dropwise. The mixture was stirred at -70° C. for a further 2 hours and at room temperature for 4 hours, cautiously treated with a saturated sodium chloride solution and taken up in ethyl acetate. The organic phase was washed with water and a saturated sodium chloride solution, dried over sodium sulfate and distilled in a bulb tube.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05728686 |
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| Source dataset | uspto-grants-1998_03 |
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| ORD ID | ord-8696035fa4f54687939bb64a88e38937 |
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| Source note | uspto-grants-1998_03 |
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