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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 130353생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/130353

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Bromodifluoromethyl diethylphosphonateHCID 144101—
반응물3-Bromo-4-iodotolueneHCID 626634—
촉매ZincHCID 23994—
촉매copper(I) bromideHCID 24593—
용매DimethylacetamideHCID 31374—
생성물Diethyl ((2-bromo-4-methylphenyl)difluoromethyl)phosphonateHCID 5218121682.3%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07381736B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-ff395510623945659e3a678161892b75
출처 메모uspto-grants-2008_06