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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Bromodifluoromethyl diethylphosphonate | HCID 144101 | — |
| Reactant | 3-Bromo-4-iodotoluene | HCID 626634 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Catalyst | copper(I) bromide | HCID 24593 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | Diethyl ((2-bromo-4-methylphenyl)difluoromethyl)phosphonate | HCID 52181216 | 82.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07381736B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-ff395510623945659e3a678161892b75 |
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| Source note | uspto-grants-2008_06 |
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