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Selectfluor → HCID 46218814, 화합물

HRID 386850
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HRID 386850 반응식
[B-](F)(F)(F)F.[B-](F)(F)(F)F.C1[N+]2(CCl)CC[N+]([F:21])(CC2)C1.[O:22]1[CH2:27][CH2:26][CH:25]([C:28]2[CH:33]=[CH:32][C:31]([OH:34])=[CH:30][C:29]=2[OH:35])[CH2:24][CH2:23]1>C(#N)C>[F:21][C:32]1[CH:33]=[C:28]([CH:25]2[CH2:24][CH2:23][O:22][CH2:27][CH2:26]2)[C:29]([OH:35])=[CH:30][C:31]=1[OH:34]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 2724933SelectfluorHCID 462078334-(tetrahydro-2H-pyran-4-yl)-1,3-benzenediol

생성물 1

HCID 46218814HCID 46218814, 화합물수율 10%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

3.65 g of N-fluoro-N′-(chloromethyl)triethylenediamine bis(tetrafluoroborate) are added to a solution of 2 g of 4-(tetrahydropyran-4-yl)benzene-1,3-diol (Example 1) in 20 ml of acetonitrile at 0° C. The reaction mixture is stirred for 16 hours at ambient temperature. The reaction mixture is extracted with ethyl acetate, and the organic phases are washed and then dried over sodium sulphate. The residue is chromatographed on silica gel (9/1 heptane/ethyl acetate). 200 mg of 4-fluoro-6-(tetrahydropyran-4-yl)benzene-1,3-diol are obtained. Yield=10%.

후처리

  1. extractionThe reaction mixture is extracted with ethyl acetate
  2. washthe organic phases are washed
  3. dry with materialdried over sodium sulphate
  4. customThe residue is chromatographed on silica gel (9/1 heptane/ethyl acetate)

출처 및 근거

ORD 기록
ord-b4dcd99fc5c24b99900d5896a52ab525
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08372879B2

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