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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271390Generated: October 31, 2026

4-Iodotoluene → Ethyl 2,2-difluoro-2-(p-tolyl)acetate

https://huagongshe.com/reaction/271390

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-IodotolueneHCID 12207—
ReactantPotassium Phosphate, DibasicHCID 24450—
ReactantEthyl bromodifluoroacetateHCID 69585—
CatalystCopperHCID 23978—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventIsopropyl AcetateHCID 7915—
ProductEthyl 2,2-difluoro-2-(p-tolyl)acetateHCID 1488869969.8%

Reaction Conditions

Temperature55 °C

Reaction Steps

The compound was prepared by modification to the procedure of Sato, K.; Kawata, R.; Ama, F.; Omote, M.; Ando, A. Chemical & Pharmaceutical Bulletin 47(7), 1013-1016 (1999). To a solution of 1-iodo-4-methylbenzene (25.1 g, 115 mmol) in DMSO (125 mL) was added ethyl bromo(difluoro)acetate (24.7 g, 122 mmol) and copper (16.8 g, 264 mmol), and the resulting solution was heated to 55° C. After 14 h the reaction was cooled to room temperature and diluted with isopropyl acetate, then cooled to 0° C. and treated with a solution of potassium hydrogen phosphate (23.3 g) in water (250 mL). The mixture was filtered through a pad of Celite, rinsing with isopropyl acetate. The phases were separated and the aqueous layer was washed with isopropyl acetate. The combined organic layers were washed with brine, dried (sodium sulfate), filtered and concentrated. The residue was purified by silica gel chromatography (5% methylene chloride, 1-8% ethyl acetate/hexanes gradient) gave the title compound (17.2 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07452893B2
Source datasetuspto-grants-2008_11
ORD IDord-7861dc9ab7ff42dfb46121eac6620463
Source noteuspto-grants-2008_11