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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28786Generated: October 26, 2026

Sulfuric Acid → Dimethyl (6-methyl-2-oxoheptyl)phosphonate

https://huagongshe.com/reaction/28786

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant5-Methylhexanoic acidHCID 12344—
ReactantDimethyl methylphosphonateHCID 12958—
ReactantMethyl 5-methylhexanoateHCID 519894—
ReactantButyllithiumHCID 178418339—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductDimethyl (6-methyl-2-oxoheptyl)phosphonateHCID 1522396876.2%

Reaction Steps

To a solution of dimethyl methylphosphonate (2.17 ml, 20 mmol) in anhydrous THF (20 mL), cooled at −78° C. was added n-BuLi (1.6 M in hexane, 13.7 mL, 22 mmol). The mixture was stirred for 30 minutes at this temperature under nitrogen. Methyl 5-methylhexanoate (1.44 g, 10 mmol), prepared from 5-methylhexanoic acid (from Avocado) and methanol at the presence of the catalytic amount of the concentrated sulfuric acid (the procedure described in Intermediate 17.1), was added dropwise for 10 minutes. The mixture was stirred for 2 hours at −78° C., gradually was warm to room temperature. The mixture was quenched with addition of 1N HCl to pH 4-5. The organic layer was separated, washed with brine and dried over MgSO4. The residue was purified through flash chromatography on silica gel (EtOAc:Hexanes=1:1) to give the product (1.80 g) with colorless oil in 76% yield. 1HNMR (CD3OD, ppm) δ 0.866 (d, J=6.5 Hz, 6H), 1.16 (m, 2H), 1.56 (m, 3H), 2.58 (t, J=7.3 Hz, 2H), 3.10 (d, J=22.7 Hz, 2H), 3.70 (s, 3H), 3.79 (s, 3H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07419999B2
Source datasetuspto-grants-2008_09
ORD IDord-002ca54a27b442f1985da6a42793eac5
Source noteuspto-grants-2008_09