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Water → HCID 58836110, 화합물

HRID 600155
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HRID 600155 반응식
Br[C:2]1[C:3]2[C:8]([C:9]([C:16]3[CH:21]=[CH:20][C:19]([CH3:22])=[CH:18][CH:17]=3)=[C:10]3[C:15]=1[CH:14]=[CH:13][CH:12]=[CH:11]3)=[CH:7][CH:6]=[CH:5][CH:4]=2.[Li]CCCC.C(O[B:32]1[O:36][C:35]([CH3:38])([CH3:37])[C:34]([CH3:40])([CH3:39])[O:33]1)(C)C.O>C1COCC1>[CH3:39][C:34]1([CH3:40])[C:35]([CH3:38])([CH3:37])[O:36][B:32]([C:2]2[C:3]3[C:8]([C:9]([C:16]4[CH:21]=[CH:20][C:19]([CH3:22])=[CH:18][CH:17]=4)=[C:10]4[C:15]=2[CH:14]=[CH:13][CH:12]=[CH:11]4)=[CH:7][CH:6]=[CH:5][CH:4]=3)[O:33]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 50177412-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 14934743HCID 14934743, 화합물HCID 178418339Butyllithium

생성물 1

HCID 58836110HCID 58836110, 화합물수율 67%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran
용매

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온도
-78 °C

실험 절차

4.6 g (1 eq, 13.25 mmol) of 9-bromo-10-p-tolyl-anthracene was dissolved in 150 ml of THF in a 500 ml round-bottomed flask in Ar gas condition, and 6.36 ml (1.2 eq, 15.9 mmol) of 2.5M n-BuLi (in hexane) was added to the solution at −78° C. After stirring the solution at −78° C. for 1 hour, 3.52 ml (1.3 eq, 17.23 mmol) of 2-isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane was added to the solution and stirred at room temperature for 2 hours. Next, 50 ml of water was added to the solution to terminate the reaction, and the organic phase of the solution was extracted using brine and methylene chloride. The extracted organic phase was dried using anhydrous magnesium sulfate and filtered to remove the solvent. The dried organic phase was dissolved in a small amount of toluene and subjected to column chromatography (silica and hexane) to remove impurities. Next, the polarity of the eluent solvent was increased to obtain 3.5 g (67%) of a white solid.

후처리

  1. additionwas added to the solution at −78° C
  2. stirringstirred at room temperature for 2 hours
  3. customto terminate
  4. customthe reaction
  5. extractionthe organic phase of the solution was extracted
  6. customThe extracted organic phase was dried
  7. filtrationfiltered
  8. customto remove the solvent
  9. dissolutionThe dried organic phase was dissolved in a small amount of toluene
  10. customto remove impurities
  11. temperatureNext, the polarity of the eluent solvent was increased

출처 및 근거

ORD 기록
ord-f4db59bbd2d0419f81a89a2b3bf28b4f
출처 데이터셋
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07901793B2

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