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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503023Generated: October 25, 2026

Hexane → Dimethyl 2-Oxo-3-methylheptylphosphonate

https://huagongshe.com/reaction/503023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantDimethyl methylphosphonateHCID 12958—
ReactantAmmonium ChlorideHCID 25517—
ReactantHexanoic acid, 2-methyl-, methyl esterHCID 519892—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductDimethyl 2-Oxo-3-methylheptylphosphonateHCID 12906670—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of dimethyl methylphosphonate (60 g, 485 mmol) in 600 ml THF was cooled to −78° C. and treated with a 2.5 M solution n-butyl lithium in hexane (194 mL, 485 mmol). After 30 min, the reaction was treated with a solution of methyl 2-methylhexanoate (14 g, 97 mmol) in THF (40 mL). The reaction was stirred for 1 h at −78° C. The reaction was treated with a saturated aqueous ammonium chloride solution (200 mL) and allowed to warm to ambient temperature. The solution was diluted with water and extracted with ether. The combined organic layers were washed with brine, dried, and concentrated. Purification by normal phase chromatography using a gradient of ethyl acetate in hexane gave dimethyl (3-methyl-2-oxoheptyl)phosphonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776896B2
Source datasetuspto-grants-2010_08
ORD IDord-64cfdb97be9e4bd0b7a3ba4e426e2e6b
Source noteuspto-grants-2010_08