HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606580Generated: October 25, 2026
CID 406 → Dimethyl (3,3-dimethyl-2-oxoheptyl)phosphonate
https://huagongshe.com/reaction/1606580
Participants
| Role | Name | HCID | Charge |
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| Reactant | CID 406 | HCID 406 | — |
| Reactant | Dimethyl methylphosphonate | HCID 12958 | — |
| Reactant | 2,2-Dimethyl-hexanoic acid methyl ester | HCID 527556 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Dimethyl (3,3-dimethyl-2-oxoheptyl)phosphonate | HCID 13018035 | — |
Reaction Steps
A solution of 18.4 g. (0.116 moles) dimethyl methylphosphonate (Aldrich) in 200 ml. dry tetrahydrofuran is cooled to -78° in a dry nitrogen atmosphere. To the stirred phosphonate solution is added 67.3 ml. of 1.90 M n-butyllithium in hexane solution (Alfa Inorganics, Inc.) dropwise over a period of 40 minutes at such a rate that the reaction temperature never rose above -65°. After an additional 5 minutes stirring at -78°, 10.2 g. (58.1 mmoles) methyl 2,2-dimethylhexanoate is added dropwise at a rate that kept the reaction temperature less than -70°(20 minutes). After 1.0 hour at -78° the reaction mixture is allowed to warm to ambient temperature, neutralized with 10 ml. acetic acid and rotary evaporated to a white gel. The gelatinous material is taken up in 75 ml. water, the aqueous phase extracted with 100 ml. portions of chloroform (3×), the combined organic extracts are backwashed (50 cc H2O), dried (MgSO4), and concentrated (water aspirator) to a crude residue and distilled (b.p. 80°-85° at 0.05 mm) to give dimethyl 2-oxo-3,3-dimethylheptylphosphonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03953466 |
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| Source dataset | uspto-grants-1976_04 |
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| ORD ID | ord-21f883bbe4b44cef9f7daa53e79aae48 |
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| Source note | uspto-grants-1976_04 |
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