HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867767Generated: October 31, 2026
Hexane → Dimethyl 4,4-dimethyl-2-oxoheptylphosphonate
https://huagongshe.com/reaction/867767
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hexane | HCID 8058 | — |
| Reactant | Dimethyl methylphosphonate | HCID 12958 | — |
| Reactant | Ethyl 3,3-dimethylhexanoate | HCID 14302176 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Dimethyl 4,4-dimethyl-2-oxoheptylphosphonate | HCID 14302177 | 79.8% |
Reaction Steps
Dimethyl methylphosphonate (11.7 g, 102 mmol) was dissolved in anhydrous THF (200 ml) and the resulting solution was cooled to -78° C. under argon atmosphere. A solution of n-butyl lithium in hexane (1.63N, 62.3 ml, 102 mmol) was added and the mixture was stirred for 30 minutes. A solution of ethyl 3,3-dimethylhexanoate (7.00 g, 40.6 mmol) in anhydrous THF (50 ml) was added to the reaction mixture at -78° C. andthe mixture was stirred for 30 minutes and then at room temperature for further 2 hours. Acetic acid was added to neutralize the solution. Water (20 ml) was added and then the solution was concentrated. The resulting residue were partitioned between ethyl acetate (200 ml) and water (10 ml). The ethyl acetate layer was separated, washed with water (80 ml) and with brine (100 ml), dried over anhydrous magnesium sulfate, and concentrated. The residue was distilled under reduced pressure to give oily product, dimethyl 4,4-dimethyl-2-oxoheptylphosphonate (8.11 g, 32.4 mmol, 79.8%, b.p.: 101°-104° C./0.03 mmHg). The structure was identified by the following data.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04775692 |
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| Source dataset | uspto-grants-1988_10 |
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| ORD ID | ord-675bd827645c445d9bfc188c42335e4a |
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| Source note | uspto-grants-1988_10 |
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