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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1-Dimethylethyl 6-formyl-2,2-dimethyl-1,3-dioxane-4-acetate | HCID 15614601 | — |
| Reactant | Dimethyl [3,3-bis(4-fluorophenyl)-2-difluoromethyl-2-propen-1-yl]phosphonate | HCID 54009116 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,1-Dimethylethyl 6-[3-difluoromethyl-4,4-bis(4-fluorophenyl)-1,3-butadienyl]-1,3-dioxane-4-acetate | HCID 53698254 | 46.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05011947 |
|---|
| Source dataset | uspto-grants-1991_04 |
|---|
| ORD ID | ord-f6efdf4cc3df4b71b32c6117ddb89c79 |
|---|
| Source note | uspto-grants-1991_04 |
|---|