Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Dimethyl methylphosphonate | HCID 12958 | — |
| Reactant | 2,2-Dimethyl-hexanoic acid methyl ester | HCID 527556 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 21412491 | HCID 21412491 | — |
Reaction Steps
Dimethyl methylphosphonate (14.88 g) is dissolved in dry tetrahydrofuran (THF, 34 ml) under a nitrogen atmosphere. The solution is cooled to -78° C. Butyllithium (7.68 g, 52 ml of 2.3 molar solution, 3 equiv.) is added very slowly during 1 hour. The mixture is stirred at -78° C for 15 minutes. A solution of 2,2-dimethylhexanoic acid methyl ester (6.32 g) in dry THF (16 ml) is added to the cold solution over a period of 1 hour. The mixture is stirred for 30 minutes and then allowed to warm up to room temperature. The reaction mixture is diluted with ether. Dilute (10%) hydrochloric acid (30 ml) is added and the reaction mixture shaken well. The organic phase is separated and washed several times with water, dried (MgSO4) and the solvent removed. The residue is distilled under reduced pressure to give the title compound, b.p. 110° - 120° C/0.1mm, γmaxfilm 1700, 1250, 1020 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04048328 |
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| Source dataset | uspto-grants-1977_09 |
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| ORD ID | ord-c44cf9a8d9244890b3e21d84c2903822 |
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| Source note | uspto-grants-1977_09 |
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