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Water → HCID 23118299, 화합물

HRID 1987780
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HRID 1987780 반응식
[N+:1]([C:4]1[C:5]([CH3:20])=[C:6]2[C:11](=[C:12]([CH3:15])[C:13]=1[CH3:14])[O:10][C:9]([CH2:17][O:18]C)([CH3:16])[CH2:8][CH2:7]2)([O-:3])=[O:2].[B].O>C(Cl)Cl>[N+:1]([C:4]1[C:5]([CH3:20])=[C:6]2[C:11](=[C:12]([CH3:15])[C:13]=1[CH3:14])[O:10][C:9]([CH2:17][OH:18])([CH3:16])[CH2:8][CH2:7]2)([O-:3])=[O:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 5462311BoronHCID 23118293HCID 23118293, 화합물

생성물 1

HCID 23118299HCID 23118299, 화합물수율 49.9%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
0 °C

실험 절차

9.5 g of 6-nitro-2-methoxymethyl-2,5,7,8-tetramethylchroman was dissolved in 80 ml of methylene chloride and 31.4 ml of a 1M boron tribromidemethylene chloride solution was added under a nitrogen gas flow at 0° C., followed by stirring at 0° C. for 3 hours. After the completion of the reaction, the reaction solution was poured into water and then extracted with chloroform. The organic layer was washed with saturated saline and then dried over anhydrous magnesium sulfate. After removing magnesium sulfate by filtration and concentrating under reduced pressure, the residue was subjected to silica gel column chromatography (hexane:ethyl acetate=2:1) to obtain 4.5 g of the objective product.

후처리

  1. customAfter the completion of the reaction
  2. extractionextracted with chloroform
  3. washThe organic layer was washed with saturated saline
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customAfter removing magnesium sulfate
  6. filtrationby filtration
  7. concentrationconcentrating under reduced pressure

출처 및 근거

ORD 기록
ord-6f47813eb5234343a6406a40cb324bd3
출처 데이터셋
uspto-grants-2009_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07553837B2

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