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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638885Generated: November 4, 2026

Hexane → HCID 15077041, compound

https://huagongshe.com/reaction/1638885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantDimethyl methylphosphonateHCID 12958—
ReactantHCID 15077044HCID 15077044—
ReactantButyllithiumHCID 178418339—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15077041HCID 15077041—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Under argon atmosphere, a solution of n-butyllithium in hexane (1.71N, 29.8 ml, 0.051 mol) was dropwise added to a solution of dimethyl methylphosphonate (6.32 g, 0.051 mol) in anhydrous THF (120 ml) with stirring at -78° C., and the mixture was stirred for 30 minutes. At -78° C., a solution of ethyl 2-methyl-4-nonynoate (4.0 g, 0.02 mol) in anhydrous THF (10 ml) was dropwise added, and the mixture was stirred for 30 minutes. Acetic acid (3.1 ml) and water (20 ml) were then added to the reaction mixture at 0° C. After concentration, water (20 ml) was added to the residue and the resulting mixture was extracted with ethyl acetate (50 ml×2). The ethyl acetate layers were combined, washed with water (20 ml) and with brine (20 ml), and dried over anhydrous sodium sulfate to concentrate. Vacuum distillation of the residue (b.p.=128°-130° C. at 0.16 mmHg) gave dimethyl 3-methyl-2-oxo-5-decynylphosphonate as a colorless, transparent oil (4.75 g, 0.0173 mol, 85% yield). The structure of this product was confirmed by the following data.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04880939
Source datasetuspto-grants-1989_11
ORD IDord-0583040c4cf74c37a96fbf456c345588
Source noteuspto-grants-1989_11