HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503023Generated: October 25, 2026
Hexane → Dimethyl 2-Oxo-3-methylheptylphosphonate
https://huagongshe.com/reaction/503023
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Dimethyl methylphosphonate | HCID 12958 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Hexanoic acid, 2-methyl-, methyl ester | HCID 519892 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Dimethyl 2-Oxo-3-methylheptylphosphonate | HCID 12906670 | — |
Reaction Steps
A solution of dimethyl methylphosphonate (60 g, 485 mmol) in 600 ml THF was cooled to −78° C. and treated with a 2.5 M solution n-butyl lithium in hexane (194 mL, 485 mmol). After 30 min, the reaction was treated with a solution of methyl 2-methylhexanoate (14 g, 97 mmol) in THF (40 mL). The reaction was stirred for 1 h at −78° C. The reaction was treated with a saturated aqueous ammonium chloride solution (200 mL) and allowed to warm to ambient temperature. The solution was diluted with water and extracted with ether. The combined organic layers were washed with brine, dried, and concentrated. Purification by normal phase chromatography using a gradient of ethyl acetate in hexane gave dimethyl (3-methyl-2-oxoheptyl)phosphonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07776896B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-64cfdb97be9e4bd0b7a3ba4e426e2e6b |
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| Source note | uspto-grants-2010_08 |
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