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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 28786Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/28786

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
Edukt5-Methylhexanoic acidHCID 12344—
EduktDimethyl methylphosphonateHCID 12958—
EduktMethyl 5-methylhexanoateHCID 519894—
EduktButyllithiumHCID 178418339—
LösungsmittelMethanolHCID 887—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktDimethyl (6-methyl-2-oxoheptyl)phosphonateHCID 1522396876,2%

Reaktionsschritte

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)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07419999B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-002ca54a27b442f1985da6a42793eac5
Quellennotizuspto-grants-2008_09