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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 527562Generated: October 30, 2026

Hexane → Ethyl (2,6-bis{[(methyloxy)methyl]oxy}phenyl)(oxo)acetate

https://huagongshe.com/reaction/527562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantEthoxalyl chlorideHCID 20884—
Reactant1,3-Bis(methoxymethoxy)benzeneHCID 12222682—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductEthyl (2,6-bis{[(methyloxy)methyl]oxy}phenyl)(oxo)acetateHCID 6723567553.1%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 1,3-bis{[(methyloxy)methyl]oxy}benzene (Intermediate 79, 2.19 g) in dry tetrahydrofuran (10 ml) at room temperature BuLi 1.6M in hexane (8.29 ml, 13.26 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 chloro(oxo)acetate (2.263 g, 16.57 mmol) in dry tetrahydrofuran (10 ml) at −78° C. The reaction mixture was stirred at −78° C. for 30 minutes. The reaction was quenched with an aqueous saturated solution of ammonium chloride (10 ml) and extracted with ethyl acetate (2×30 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 as a light yellow oil (1.75 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346790B2
Source datasetuspto-grants-2016_05
ORD IDord-6d68b139a2c24b4799b8a38a9167e668
Source noteuspto-grants-2016_05