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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1484628Generated: October 30, 2026

Hexane → Ethyl 2-[2,6-bis(methoxymethoxy)-3-methyl-phenyl]-2-oxo-acetate

https://huagongshe.com/reaction/1484628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantEthoxalyl chlorideHCID 20884—
Reactant2,4-Bis(methoxymethoxy)-1-methylbenzeneHCID 67958833—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-[2,6-bis(methoxymethoxy)-3-methyl-phenyl]-2-oxo-acetateHCID 6795834757.4%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 2,4-bis(methoxymethoxy)-1-methyl-benzene (Intermediate 7, 5.5 g, 25.94 mmol) in dry tetrahydrofuran (50 ml) at room temperature BuLi 1.6M in hexane (19.45 ml, 31.13 mmol) was added and the reaction mixture was stirred for 30 minutes at the same temperature. The mixture was cooled to −78° C. and it was added (via cannulation) to a solution of ethyl chlorooxoacetate (4.35 ml, 38.9 mmol) in dry tetrahydrofuran (30 ml) at −78° C. The reaction mixture was stirred at −78° C. for 30 minutes. The reaction was quenched with water (20 ml), diluted with brine (50 ml) and extracted with ethyl acetate (2×100 ml). Combined organic layers were dried over sodium sulphate, filtered and evaporated. The residue was purified by flash chromatography (Biotage system) on silica gel using a 100 g SNAP column and cyclohexane to cyclohexane/ethyl acetate 8:2 as eluent affording the title compound (4.65 g) as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422272B2
Source datasetuspto-grants-2016_08
ORD IDord-f772a3af28b64d19b0163f70e7d51599
Source noteuspto-grants-2016_08