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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867768Generated: October 30, 2026

Hexane → HCID 14302179, compound

https://huagongshe.com/reaction/867768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantDimethyl methylphosphonateHCID 12958—
ReactantHCID 14302178HCID 14302178—
ReactantButyllithiumHCID 178418339—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14302179HCID 1430217971.1%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Dimethyl methylphosphonate (5.89 g, 47.5 mmol) was dissolved in anhydrous THF (80 ml). To the resulting solution cooled to -78° C. under argon atomosphere, a solution of n-butyl lithium in hexane (1.63N, 29.1 ml, 47.5 mmol) was added and the mixture was stirred for 30 minutes. A solution of methyl 4,4-dimethylhexanoate (3.00 g, 19.0 mmol) in anhydrous THF (15 ml) was then added to the reaction mxiture at -78° C. and the mixture was stirred for 30 minutes. After warming the mixture to room temperature, acetic acid was added to neutralize the solution and a small quantity of water was then added, and concentrated. After ethyl acetate was added to the residue, the ethyl acetate layer was washed with water and with brine, dried over anhydrous magnesium sulfate, and concentrated. The residue was distilled under reduced pressure to give oily product, dimethyl 5,5-dimethyl-2-oxoheptylphosphonate (3.38 g, 13.5 mmol, 71.1%, b.p.: 120°-122° C./0.18 mmHg). The structure was confirmed by the following data.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04775692
Source datasetuspto-grants-1988_10
ORD IDord-3f94f3d776d047d6a27038c9b2b97271
Source noteuspto-grants-1988_10