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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130353Generated: October 25, 2026

Water → Diethyl ((2-bromo-4-methylphenyl)difluoromethyl)phosphonate

https://huagongshe.com/reaction/130353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBromodifluoromethyl diethylphosphonateHCID 144101—
Reactant3-Bromo-4-iodotolueneHCID 626634—
CatalystZincHCID 23994—
Catalystcopper(I) bromideHCID 24593—
SolventDimethylacetamideHCID 31374—
ProductDiethyl ((2-bromo-4-methylphenyl)difluoromethyl)phosphonateHCID 5218121682.3%

Reaction Steps

A solution of (bromo-difluoro-methyl)-phosphonic acid diethyl ester (25.00 g, 93.6 mmol) in N,N-dimethylacetamide (50 mL) was added drop wise into a suspension of activated zinc (6.12 g, 93.6 mmol) under Argon. The reaction was initiated by heating and kept under 50° C. After the mixture was stirred for 3 h, copper (I) bromide (13.43 g, 93.6 mmol) was added and stirred for 1 h. A solution of 2-bromo-1-iodo-4-methyl-benzene (11.88 g, 40.0 mmol) in N,N-dimethylacetamide (25 mL) was added slowly to the reaction mixture. The resulting suspension was then stirred at room temp for 18 h. Water (100 mL) was added to the reaction mixture and the solution filtered through celite. The filtrate was diluted with EtOAc (250 mL) and organic layer was washed with H2O (50 mL), NaHCO3 (5%, 50 mL) and H2O (50 mL). The solvent was removed and the residue was purified by column chromatography on silica gel, eluting with hexanes/EtOAc (4:1) to provide a colorless oil (11.75 g, 82%): 1H NMR (300 MHz, CDCl3) δ 7.51 (d, 1H), 7.49 (s, 1H), 7.19 (d, 1H), 4.26 (m, 4H), 2.36 (s, 3H), 1.48 (s, 9H), 137 (m, 6 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07381736B2
Source datasetuspto-grants-2008_06
ORD IDord-ff395510623945659e3a678161892b75
Source noteuspto-grants-2008_06