Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233769Generated: October 29, 2026

Ammonium Chloride → Tert-butyl 2,4-difluoro-3-vinylbenzoate

https://huagongshe.com/reaction/2233769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantMethyltriphenylphosphonium iodideHCID 638159—
ReactantTert-butyl 2,4-difluoro-3-formylbenzoateHCID 86626216—
ReactantHCID 178420697HCID 178420697—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 2,4-difluoro-3-vinylbenzoateHCID 6845130350%

Reaction Conditions

Temperature0 °C

Reaction Steps

At −78° C., 9.50 ml of 1.59 M n-butyl lithium-THF solution was added dropwise to 90 ml of THF solution containing 8.13 g of methyltriphenylphosphonium iodide. This was stirred at 0° C. for 10 minutes, cooled to −78° C. and then mixed with 2.44 g of tert-butyl 2,4-difluoro-3-formylbenzoate dissolved in 10 ml of THF. After 40 minutes thereof, this was stirred at room temperature for 1 hour, mixed with appropriate amounts of saturated ammonium chloride aqueous solution and purified water, extracted with ethyl acetate and then dried with anhydrous magnesium sulfate. After concentration, the thus formed residue was purified by a silica gel column chromatography to obtain 1.20 g (50%) of tert-butyl 2,4-difluoro-3-vinylbenzoate (Reference Example 5-1) from a hexane-ethyl acetate (50:1) eluate. ES−: 239

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709519B2
Source datasetuspto-grants-2010_05
ORD IDord-6844445b3fb140778e4764510d4da8c6
Source noteuspto-grants-2010_05