Triethylamine → Diisopropyl P-[[(2-(difluoromethoxy)-6-methylphenyl)sulfonyloxy]methyl]phosphonate
반응식
[OH:1][CH2:2][P:3](=[O:12])([O:8][CH:9]([CH3:11])[CH3:10])[O:4][CH:5]([CH3:7])[CH3:6].C(N(CC)CC)C.[CH3:20][C:21]1[CH:26]=[CH:25][CH:24]=[C:23]([O:27][CH:28]([F:30])[F:29])[C:22]=1[S:31](Cl)(=[O:33])=[O:32]>CCOCC.C(OCC)(=O)C.C(Cl)Cl>[F:30][CH:28]([F:29])[O:27][C:23]1[CH:24]=[CH:25][CH:26]=[C:21]([CH3:20])[C:22]=1[S:31]([O:1][CH2:2][P:3](=[O:12])([O:4][CH:5]([CH3:7])[CH3:6])[O:8][CH:9]([CH3:11])[CH3:10])(=[O:33])=[O:32]참가 물질
반응물 3
생성물 1
시약·촉매·용매 3
실험 절차
A solution of 20 ml of ether, 8.6 g of diisopropyl P-(hydroxymethyl)phosphonate, prepared in Example 17, and 6.9 ml of triethylamine was added dropwise over 25 minutes to 15.2 g of crude 2-methyl-6-(difluoromethoxy)benzenesulfonyl chloride, prepared in Example 3, in 70 ml of ether. After the mild exotherm, the reaction was allowed to stir overnight at room temperature and was then diluted with 200 ml of ethyl acetate, the resulting ethyl acetate solution washed with two 80 ml portions of water, dried with magnesium sulfate, filtered, and concentrated to yield 10.2 g of the very crude desired product as a black oil. The crude product was dissolved in 10 ml of methylene chloride and flash chromatographed on Merck silica gel using ethyl acetate and hexanes. After combining similar fractions, the desired product was isolated as an amber oil in low yield.
후처리
- washthe resulting ethyl acetate solution washed with two 80 ml portions of water
- dry with materialdried with magnesium sulfate
- filtrationfiltered
- concentrationconcentrated
- customto yield 10.2 g of the very crude desired product as a black oil
- customflash chromatographed on Merck silica gel
출처 및 근거
- ORD 기록
- ord-347013a9bcfd4327a908a0f0c94d540e
- 출처 데이터셋
- uspto-grants-1993_12
- 특허 번호
- US05272128
반응 노트
불러오는 중…