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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 527563Generated: October 30, 2026

Potassium bis(trimethylsilyl)amide → Ethyl 2-(2,6-bis{[(methyloxy)methyl]oxy}phenyl)-2-propenoate

https://huagongshe.com/reaction/527563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantEthyl (2,6-bis{[(methyloxy)methyl]oxy}phenyl)(oxo)acetateHCID 67235675—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-(2,6-bis{[(methyloxy)methyl]oxy}phenyl)-2-propenoateHCID 6723518379.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of methyltriphenylphosphonium bromide (3.13 g, 8.75 mmol) in dry tetrahydrofuran (30 ml) at 0° C. KHMDS (1.745 g, 8.75 mmol) was slowly added and the reaction mixture was stirred for 15 minutes at 0° C. and for 45 minutes at room temperature. The reaction mixture was cooled to 0° C. and a solution of ethyl (2,6-bis{[(methyloxy)methyl]oxy}phenyl)(oxo)acetate (Intermediate 80, 1.74 g) in dry tetrahydrofuran (10 mL) was slowly added and the reaction mixture was stirred for 2 hours at 0° C. The reaction was quenched with an aqueous saturated solution of ammonium chloride (10 ml), diluted with water (20 ml) and extracted with ethyl acetate (2×50 ml). The organic layer was 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 eluents affording the title compound as a colourless oil (1.37 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346790B2
Source datasetuspto-grants-2016_05
ORD IDord-6fb45df2989841b9984af0f4fad44666
Source noteuspto-grants-2016_05