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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086100Generated: November 3, 2026

1,1-Dimethylethyl 6-formyl-2,2-dimethyl-1,3-dioxane-4-acetate → 1,1-Dimethylethyl 6-[3-difluoromethyl-4,4-bis(4-fluorophenyl)-1,3-butadienyl]-1,3-dioxane-4-acetate

https://huagongshe.com/reaction/1086100

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-Dimethylethyl 6-formyl-2,2-dimethyl-1,3-dioxane-4-acetateHCID 15614601—
ReactantDimethyl [3,3-bis(4-fluorophenyl)-2-difluoromethyl-2-propen-1-yl]phosphonateHCID 54009116—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1,1-Dimethylethyl 6-[3-difluoromethyl-4,4-bis(4-fluorophenyl)-1,3-butadienyl]-1,3-dioxane-4-acetateHCID 5369825446.9%

Reaction Steps

Butyl lithium (1.04 mL of 2.5M solution, 2.6 mmol) was added to a solution of dimethyl [3,3-bis(4-fluorophenyl)-2-difluoromethyl-2-propen-1-yl]phosphonate (1.0 g, 2.6 mmol) in 10 mL of tetrahydrofuran at -78° C. After stirring for 30 minutes, 1,1-dimethylethyl 6-formyl-2,2-dimethyl-1,3-dioxane-4-acetate (0.82 g, 3.2 mmol) was added and the mixture stirred for 64 hrs. at room temperature. The mixture was quenched with saturated ammonium chloride solution and extracted with diethyl ether. The extracts were dried over magnesium sulfate and conentrated in vacuo. The residue was purified by chromatography on silica eluting with 5% ethyl acetate in hexane to give an oil. Crystallization from pentane gave 0.6 g of the title compound; m.p. =124°-125° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05011947
Source datasetuspto-grants-1991_04
ORD IDord-f6efdf4cc3df4b71b32c6117ddb89c79
Source noteuspto-grants-1991_04