Imidazole → HCID 57912293, 화합물

HRID 340849노트

반응식

HRID 340849 반응식
[N+:1]([C:4]1[C:9]([CH2:10][OH:11])=[CH:8][CH:7]=[CH:6][C:5]=1[CH2:12][OH:13])([O-:3])=[O:2].CN(C=O)C.N1C=CN=C1.[Si:24](Cl)([C:27]([CH3:30])([CH3:29])[CH3:28])([CH3:26])[CH3:25]>C(OCC)(=O)C>[Si:24]([O:13][CH2:12][C:5]1[C:4]([N+:1]([O-:3])=[O:2])=[C:9]([CH2:10][OH:11])[CH:8]=[CH:7][CH:6]=1)([C:27]([CH3:30])([CH3:29])[CH3:28])([CH3:26])[CH3:25]

참가 물질

6

반응물 4

HCID 795ImidazoleHCID 6228DimethylformamideHCID 28928tert-Butyldimethylsilyl chlorideHCID 13519807[3-(hydroxymethyl)-2-nitrophenyl]methanol

생성물 1

HCID 57912293HCID 57912293, 화합물수율 80%

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

To a clean, dry round-bottom flask was added 2-nitro-1,3-benzenedimethanol (818 mg, 4.47 mmol), anhydrous DMF (40 mL), and imidazole (304.2 mg, 4.47 mmol). The solution was maintained at 0° C. while tert-butyldimethylsilylchloride (337 mg, 2.24 mmol) was slowly added. The resulting pale yellow solution was allowed to warm to room temperature and stirred overnight under argon before being diluted with ethyl acetate (100 mL), washed with water (5×50 mL), dried over MgSO4, filtered, concentrated on a rotary evaporator, and purified by silica gel chromatography (30% EtOAc:hexanes) to yield 3-(tert-butyldimethylsilyloxymethyl)-2-nitro-hydroxymethylbenzene as a yellow oil which crystallized upon further solvent removal in vacuo. The excess 2-nitro-1,3-benzenedimethanol was recovered and re-subjected to the reaction conditions to yield Compound 9 in 80% yield after three iterations.

후처리

  1. additionwas slowly added
  2. washwashed with water (5×50 mL)
  3. dry with materialdried over MgSO4
  4. filtrationfiltered
  5. concentrationconcentrated on a rotary evaporator
  6. custompurified by silica gel chromatography (30% EtOAc:hexanes)

출처 및 근거

ORD 기록
ord-d63c752a443e4f7cba10a6293ab29441
출처 데이터셋
uspto-grants-2014_11
특허 번호
US08895673B2

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